Publications from the Jung Group

1. G. Stork, and M. E. Jung, "Vinylsilanes as Carbonyl Precursors. Use in Annelation Reactions," J. Am. Chem. Soc. 1974, 96, 3682-3684. [pdf]

2. G. Stork, M. E. Jung, E. Colvin, and Y. Noel, "Synthetic Routes to Halomethyl Vinylsilanes," J. Am. Chem. Soc. 1974, 96, 3684-3686. [pdf]

3. M.E. Jung, "I. Trans, trans-1,4-Diacetoxy-2-Methyl-1,3-Butadiene. A Possible Starting Material for Tetrodotoxin; II. Vinylsilanes as Annelation Reagents," Diss. Abstr. Int. B 1974, 34, 4288. [pdf]

4. M. E. Jung, "Stereoselective Synthesis of Substituted Functionalized Butadienes," J. Chem. Soc., Chem. Commun. 1974, 956-957. [pdf]

5. M. E. Jung, "A Review of Annulation," Tetrahedron 1976, 32, 3-30. [pdf]

6. M. E. Jung, "Oxidation of Trimethylsilyl Ethers via Hydride Abstraction: A New Procedure for Alcohol Oxidation," J. Org. Chem. 1976, 41, 1479-1480. [pdf]

7. M. E. Jung, P. A. Blair, and J. A. Lowe, "Reactions of Oxime Dianions: Stereospecificity in Alkylation," Tetrahedron Lett. 1976, 1439-1442. [pdf]

8. M. E. Jung and C. A. McCombs, "2-Trimethylsilyloxy-1,3-Butadiene. A New Reactive Diene. Preparation and Reactions," Tetrahedron Lett. 1976, 2935-2938. [pdf]

9. O. L. Chapman, C.-C. Chang, J. Kolc, M. E. Jung, J. A. Lowe, T. J. Barton, and M. L. Tumey, "1,1,2-Trimethylsilaethylene," J. Am. Chem. Soc. 1976, 98, 7844-7846. [pdf]

10. M. E. Jung and L. M. Speltz, "Oxidation of Ethers via Hydride Abstraction: A New Procedure for Selective Oxidation of Primary, Secondary Diols at the Secondary Position," J. Am. Chem. Soc. 1976, 98, 7882-7884. [pdf]

11. M. E. Jung and M. A. Lyster, "Quantitative Dealkylation of Alkyl Esters via Treatment with Trimethylsilyl Iodide. A New Method for Ester Hydrolysis," J. Am. Chem. Soc. 1977, 99, 968-969. [pdf]

12. M. E. Jung and J. A. Lowe, "Synthetic Approaches to Adriamycin Involving Diels-Alder Reactions of Photochemically Generated Bis-Ketenes: Total Synthesis of Islandicin and Digitopurpone," J. Org. Chem. 1977, 42, 2371-2373. [pdf]

13. M. E. Jung and P. L. Ornstein, "A New Method for the Efficient Conversion of Alcohols into Iodides via Treatment with Trimethylsilyl Iodide," Tetrahedron Lett. 1977, 2659-2662. [pdf]

14. M. E. Jung and J. P. Hudspeth, "Three-Carbon Annulation. Formation of Five-Membered Rings from Olefins via Diels-Alder Reaction," J. Am. Chem. Soc. 1977, 99, 5508-5510. [pdf]

15. M. E. Jung and T. J. Shaw, "Stereospecificity in Alkylation of Anions of Ketone Dimethylhydrazones: Kinetic Anti Preference, Thermodynamic Syn Preference," Tetrahedron Lett. 1977, 3305-3308. [pdf]

16. M. E. Jung and R. B. Blum, "Generation of the Enolate of Acetaldehyde from Non-Carbonyl Substances and its C-Alkylation, O-Acylation, and O-Silylation," Tetrahedron Lett. 1977, 3791-3794. [pdf]

17. M. E. Jung and M. A. Lyster, "Quantitative Dealkylation of Alkyl Ethers via Treatment with Trimethylsilyl Iodide. A New Method for Ether Hydrolysis," J. Org. Chem. 1977, 42, 3761-3764. [pdf]

18. M. E. Jung, W. A. Andrus, and P. L. Ornstein, "Non-Aqueous Conversion of Ketals to Ketones via Treatment with Trimethylsilyl Iodide," Tetrahedron Lett. 1977, 4175-4178. [pdf]

19. M. E. Jung, Y.-G. Pan, M. W. Rathke, D. F. Sullivan, and R. P. Woodbury, "Oxidation of Trialkylsilyl Enol Ethers via Hydride Abstraction: A New Procedure for Ketone to Enone Conversion," J. Org. Chem. 1977, 42, 3961-3963. [pdf]

20. M. E. Jung and J. A. Lowe, "Synthetic Approaches to Aclacinomycin and Pyrromycin Antitumor Antibiotics via Diels-Alder Reactions of 6-Alkoxy-2-pyrones: Total Synthesis of Chrysophanol, Helminthosporin, and Pachybasin," J. Chem. Soc., Chem. Commun. 1978, 95-96. [pdf]

21. M. E. Jung and M. A. Lyster, "Conversion of Alkyl Carbamates to Amines via Treatment with Trimethylsilyl Iodide," J. Chem. Soc., Chem. Commun. 1978, 315-6. [pdf]

22. M. E. Jung and J. P. Hudspeth, "Anionic Oxy-Cope Rearrangements with Aromatic Substrates in Bicyclo[2.2.1] heptene Systems: Facile Synthesis of cis-Hydrindanone Derivatives, Including Steroid Analogues," J. Am. Chem. Soc. 1978, 100, 4309-4311. [pdf]

23. M. E. Jung, M. A. Mazurek, and R. M. Lim, "A New Efficient Synthesis of Iodomethyl Methyl Ether," Synthesis 1978, 588-590. [pdf]

24. M. E. Jung and R. W. Brown, "Direct Oxidation of Alcohols and Diols via Hydride Abstraction," Tetrahedron Lett. 1978, 2771-2774. [pdf]

25. M. E. Jung and C. A. McCombs, "Total Synthesis of (±) Seychellene: Use of Silyloxydienes in Synthesis," J. Am. Chem. Soc. 1978, 100, 5207-5209. [pdf]

26. M. E. Jung, A. B. Mossman, and M. A. Lyster, "Direct Synthesis of Dibenzocycloocta-octadienes via Double Ortho Friedel-Crafts Alkylation by the Use of Aldehyde-Trimethylsilyl Iodide Adducts," J. Org. Chem. 1978, 43, 3698-3701. [pdf]

27. M. E. Jung and T. A. Blumenkopf, "Mild Methods for the in situ Generation of Trimethylsilyl Iodide," Tetrahedron Lett. 1978, 3657-3660. [pdf]

28. M. E. Jung and G. L. Hatfield, "Preparation of Bromides from Alcohols via Treatment with Trimethylsilyl Bromide," Tetrahedron Lett. 1978, 4483-4486. [pdf]

29. M. E. Jung and C. A. McCombs, "2-Trimethylsilyloxy-1,3-butadiene," Organic Syntheses 1978, 58, 163-168. [pdf]

30. M. E. Jung and B. J. Gaede, "Synthesis and Diels-Alder Reactions of E-1-Trimethylsilyl-1,3-butadiene," Tetrahedron 1979, 35, 621-625. [pdf]

31. M. E. Jung, T. J. Shaw, R. R. Fraser, J. Banville, and K. Taymaz, "Reinvestigation of the Regioselectivity of Deprotonation of Ketone Dimethylhydrazones," Tetrahedron Lett. 1979, 4149-4152. [pdf]

32. M. E. Jung and M. A. Lyster, "The Cleavage of Methyl Ethers, Using Iodotrimethylsilane: Cyclohexanol from Cyclohexyl Methyl Ether," Organic Syntheses 1979, 59, 35-41. [pdf]

33. M. E. Jung and J. P. Hudspeth, "Total Synthesis of (±)-Coronafacic Acid: Use of Anionic Oxy-Cope Rearrangements on Aromatic Substrates in Synthesis," J. Am. Chem. Soc. 1980, 102, 2463-2464. [pdf]

34. M. E. Jung and T. J. Shaw, "Total Synthesis of (R)-Glycerol Acetonide and the Anti-epileptic and Hypotensive Drug, (-)-γ-Amino-β-hydroxybutyric Acid (GABOB): Use of Vitamin C as a Chiral Starting Material," J. Am. Chem. Soc. 1980, 102, 6304-6311. [pdf]

35. M. E. Jung and Y.-G. Pan, "Direct Stereoselective Total Synthesis of (±)-Seychellene," Tetrahedron Lett. 1980, 21, 3127-3130. [pdf]

36. M. E. Jung and C. D. Radcliffe, "Total Synthesis of the Sesquiterpene (±)-β-Cuparenone: Use of Three-Carbon Annulation in Synthesis," Tetrahedron Lett. 1980, 21, 4397-4400. [pdf]

37. M. E. Jung and J. J. Shapiro, "Synthesis and Structure Determination of 2-Azabicyclo-[2.2.1]hept-2-enes and Their Derivatives: W Effect on Chemical Shifts," J. Am. Chem. Soc. 1980, 102, 7862-7866. [pdf]

38. M. E. Jung and S. J. Miller, "Total Synthesis of Isopavine and Intermediates for the Preparation of Substituted Amitriptyline Analogues: Facile Routes to Substituted Dibenzocyclooctatrienes and Dibenzocycloheptatrienes," J. Am. Chem. Soc. 1981, 103, 1984-1992. [pdf]

39. M. E. Jung and K. M. Halweg, "Intramolecular Lewis-Acid Promoted [2+2] Cycloadditions: An Efficient Total Synthesis of (±)-Coronafacic Acid via an Internal Diels-Alder Reaction," Tetrahedron Lett. 1981, 22, 2735-2738. [pdf]

40. M. E. Jung and R. W. Brown, "Regiospecific Friedel-Crafts Acylation of 6-Alkoxy-2-Pyrones: Preparation of Substituted Aromatics and Anthraquinones," Tetrahedron Lett. 1981, 22, 3355-3358. [pdf]

41. M. E. Jung and R. B. Blum, "Photochemical Transformation of Methoxyphthalaldehydic Esters: Synthesis of Methyl 6-Methoxyphthalaldehydate from the 3-Methoxy Isomer," J. Chem. Soc., Chem. Commun. 1981, 962-963. [pdf]

42. M. E. Jung, C. A. McCombs, Y. Takeda, and Y.-G. Pan, "Use of Silyloxydienes in Synthesis. Total Syntheses of the Sesquiterpene (±)-Seychellene," J. Am. Chem. Soc. 1981, 103, 6677-6687. [pdf]

43. M. E. Jung and K. M. Halweg, "Simple Regioselective Synthesis of Trans-7α-Methyl-hydrind-4-en-1-one, A Key Intermediate for Steroid Total Synthesis," Tetrahedron Lett. 1981, 22, 3929-3932. [pdf]

44. M. E. Jung, K. Shishido, L. Light, and L. Davis, "Preparation of Di- and Triacylimines and Their Use in the Synthesis of Nitrogen Heterocycles," Tetrahedron Lett. 1981, 22, 4607-4610. [pdf]

45. M. E. Jung, K. Shishido, and L. H. Davis, "Simple Syntheses of Diethyl Oxomalonate and Alkyl Glyoxylates," J. Org. Chem. 1982, 47, 891-892. [pdf]

46. M. E. Jung and L. A. Light, "Intramolecular Diels-Alder Cycloadditions of Perchloroallyloxy- and diallyloxycyclopentadienes," J. Org. Chem. 1982, 47, 1084-1087. [pdf]

47. M. E. Jung, M. Node, R. Pfluger, M. A. Lyster, and J. A. Lowe, III, "Regiospecific Synthesis of Bicyclic 6-Alkoxy-2-Pyrones and Their Use in the Production of Tetracyclic Inter-mediates for 11-Desoxyanthracycline Synthesis," J. Org. Chem. 1982, 47, 1150-1152. [pdf]

48. M. E. Jung and L. A. Light, "Preparation of Iodoallylic Alcohols via Hydrostannylation: Spectroscopic Proof of Structures," Tetrahedron Lett. 1982, 23, 3851-3854. [pdf]

49. M. E. Jung and G. L. Hatfield, "Novel Oxidative Rearrangement of α,β-Unsaturated Ketone Hydrazones on Iodination in Base," Tetrahedron Lett. 1982, 23, 3991-3994. [pdf]

50. M. E. Jung and P. Lewis, "Addition of Organocuprates to Aldehydes via their Trimethylsilyl Iodide Adducts," Synth. Commun. 1983, 13, 213-218. [pdf]

51. M. E. Jung, "New Approaches to the Total Synthesis of Biologically Active Natural Products," in Current Trends in Organic Synthesis, IUPAC, ed. H. Nozaki, Pergamon Press, Oxford, 1983, 61-70. [pdf]

52. M. E. Jung and G. L. Hatfield, "Synthesis of Syn-7-benzyloxy-4-methylbicyclo[2.2.1]-hept-5-en-2-one, an Intermediate for the Synthesis of Steroids and Tricothecanes; Tandem Anionic [1,3]-[3,3] Sigmatropic Rearrangement," Tetrahedron Lett. 1983, 24, 2931-2934. [pdf]

53. M. E. Jung and G. L. Hatfield, "Facile Synthesis of (3aS)-1,3a-Dimethyl-2,3,3a,5,6,7-hexahydroinden-4(5H)-one, an Intermediate for Steroid Synthesis," Tetrahedron Lett. 1983, 24, 3175-3178. [pdf]

54. M. E. Jung, J. A. Hagenah, and Zeng L.-M., "Simple, Stereospecific Preparation of Z-3-Iodoacrylic Acid from Propiolic Acid and Methylmagnesium Iodide," Tetrahedron Lett. 1983, 24, 3973-3974. [pdf]

55. M. E. Jung and Zeng L.-M., "Reaction of Oximes with Trimethylsilyl Iodide: Dehydration and Beckmann Rearrangement," Tetrahedron Lett. 1983, 24, 4533-4534. [pdf]

56. M. E. Jung and J. A. Hagenah, "Mechanism of Bromination of 1,5-Diacetoxynaphthalene," J. Org. Chem. 1983, 48, 5359-5361. [pdf]

57. M. E. Jung and K. M. Halweg, "Stereoselectivity in Intramolecular Diels-Alder Reactions: A Short Total Synthesis of (±)-Estrone," Tetrahedron Lett. 1984, 25, 2121-2124. [pdf]

58. M. E. Jung and J. C. Rohloff, "Intramolecular Diels-Alder Chemistry of Pyrroles," J. Chem. Soc., Chem. Commun. 1984, 630-632. [pdf]

59. M. E. Jung, R. W. Brown, J. A. Hagenah, and C. E. Strouse, "Cycloadditions of Benzopyrones: Rapid Access to Bicyclic AB-Ring Analogues of Anthracyclines," Tetrahedron Lett. 1984, 25, 3659-3662. [pdf]

J. Am. Chem. Soc. 1984, 106, 7614-7618. [pdf]

61. M. E. Jung, J. A. Lowe, III, M. A. Lyster, M. Node, R. W. Pfluger, and R. W. Brown, "Regiospecific Synthesis of Mono- and Bicyclic 6-Alkoxy-2-pyrones and their Use in the Preparation of Substituted Aromatics, Anthraquinones, and Tetracyclic Intermediates for 11-Deoxyanthracycline Synthesis," Tetrahedron Symposium-in-Print No. 17, Tetrahedron 1984, 40, 4751-4766. [pdf]

62. M. E. Jung and L. J. Street, "Synthetic Studies on the Avermectins: Substituent Effects on Intramolecular Diels-Alder Reactions of N-Furfuryl Acrylamides and Further Reactions of the Cycloadducts," J. Am. Chem. Soc. 1984, 106, 8327-8328. [pdf]

63. M. E. Jung, P. S. Y. Lam, M. M. Mansuri, and L. M. Speltz, "Stereoselective Synthesis of an Analogue of Podophyllotoxin by an Intramolecular Diels-Alder Reaction," J. Org. Chem. 1985, 50, 1087-1094. [pdf]

64. M. E. Jung and L. J. Street, "Novel Rearrangements of 7-Oxanorbornene Systems," Tetrahedron Lett. 1985, 26, 3639-3642. [pdf]

65. M. E. Jung and J. C. Rohloff, "Organic Chemistry of L-Tyrosine. 1. General Synthesis of Chiral Piperazines from Amino Acids," J. Org. Chem. 1985, 50, 4909-4913. [pdf]

66. M. Fintel, G. A. Langer, J. C. Rohloff, and M. E. Jung, "Contribution of Myocardial Diffuse Double-layer Calcium to Contractile Function," Am. J. Physiol. 1985, 249 (Heart Circ. Physiol. 18), H989-H994. [pdf]

67. M. E. Jung and K. R. Buszek, "Alkenyltrialkylammonium Salts as Dienophiles in Diels-Alder Reactions: Preparation, Cycloadditions, and Further Reactions. β-Dimethylamino acrylonitrile Equivalent in Cycloadditions," J. Org. Chem. 1985, 50, 5440-5441. [pdf]

68. M. E. Jung, L. J. Street, and Y. Usui, "Chemoselective Cycloadditions of 3,4-Dialkoxy-furans and Alkyl Coumalates. Novel Loss of Aromaticity of Two Non-Benzenoid Aromatic Rings in a Mild Thermal Process," J. Am. Chem. Soc. 1986, 108, 6810-6811. [pdf]

69. M. E. Jung and G. T. Lowen, "A Direct Synthesis of Trans 2-Arylbenzocyclobutenol, a Potential Intermediate for Podophyllotoxin Synthesis: Use of LDA for Benzyne Formation and Trapping," Tetrahedron Lett. 1986, 27, 5319-5322. [pdf]

70. M. E. Jung and K. R. Buszek, "Alkenylimmonium Salts as Dienophiles in Diels-Alder Cycloadditions with High Reactivity and Stereoselectivity," Tetrahedron Lett. 1986, 27, 6165-6168. [pdf]

71. M. E. Jung and C.-Y. Liu, "Efficient Synthesis of a Head-to-head Isoprenoid Geochemical Biomarker from Phytol," J. Org. Chem. 1986, 51, 5446-5447. [pdf]

72. M. E. Jung and J. A. Hagenah, "Preparation and Cycloaddition of Functionalized 4,6-Dialkylpyrone-5-carboxylates. Synthesis of Bicyclic Lactones and Substituted Benzoates," Heterocycles 1987, 25, 117-121. [pdf]

73. M. E. Jung and J. A. Hagenah, "Synthetic Approach to Aklavinone Using 2-Oxo-2H-pyran-5-carboxylate (Coumalate) Intermediates," J. Org. Chem. 1987, 52, 1889-1901. [pdf]

74. M. E. Jung and D. D. Grove, "Nitroacetylene Equivalents. Preparation and Cycloadditions of 2-Phenylsulphinyl-1-nitroalkenes," J. Chem. Soc., Chem. Commun. 1987, 753-755. [pdf]

75. M. E. Jung and B. E. Love, "Syntheses and Properties of Cyclic Keto Alkenylammonium Salts," J. Chem. Soc., Chem. Commun. 1987, 1288-1289. [pdf]

76. M. E. Jung, D. D. Grove, and S. I. Khan, "Simple Preparation of α-Acyl γ-Thioaryl Oximes (N-Hydroxy 2-Oxoalkanimidothioates); Ambident Reactivity of α-Nitroketones," J. Org. Chem. 1987, 52, 4570-4573. [pdf]

77. M. E. Jung, Y. Usui, and C. T. Vu, "Rapid and Efficient Synthesis of a Fully Functionalized Synthon for the Bottom Half of the Antiparasitic Agent, Ivermectin," Tetrahedron Lett. 1987, 28, 5977-5980. [pdf]

78. M. E. Jung and S. Abrecht, "Improved Synthesis of 3-Substituted 7-Methoxybenzofurans, Useful Intermediates for the Preparation of Morphine Analogues," J. Org. Chem. 1988, 53, 423-426. [pdf]

79. M. E. Jung and L. J. Street, "Synthetic Approach to the Ivermectin Bottom Half Using Internal Cycloadducts of N-Furfuryl Acrylamides: Functionality and Optical Activity," Heterocycles 1988, 27, 45-48. [pdf]

80. M. E. Jung and H. Xia, "Synthesis and Transport Properties of 12-Silacrown-3, a New Type of Anion Complexing Agent," Tetrahedron Lett. 1988, 29, 297-300. [pdf]

81. M. E. Jung and K. R. Buszek, "The Stereochemistry of Addition of Trialkylammonium and Pyridinium Tetrafluoroborate Salts to Activated Acetylenes. Preparation of Novel Dienophiles for Diels-Alder Reactions," J. Am. Chem. Soc. 1988, 110, 3965-9. [pdf]

82. M. E. Jung and J. Gervay, "Studies on the Effects of Substituents on Rate Enhancements in Intramolecular Diels-Alder Reactions: Reasons for the Gem-Dimethyl Effect," Tetrahedron Lett. 1988, 29, 2429-2432. [pdf]

83. M. E. Jung and Y. H. Jung, "Total Synthesis of the Aglycone of the 8-Methyl Benzonaphthopyrone Antibiotics, Gilvocarcin M, Virenomycin M, and Albacarcin M," Tetrahedron Lett. 1988, 29, 2517-2520. [pdf]

84. M. E. Jung, "Problem Solving in Organic Synthesis. The False Steps, Failed Pathways, and Ultimately Successful Route to the Bottom Half of Ivermectin," in Strategies and Tactics in Organic Synthesis, Vol. 2, Ed. T. Lindberg, Academic Press, New York, 1988, Chapter 7, pp 221-261. [pdf]

85. M. E. Jung and C. T. Vu, "Intramolecular Diels-Alder Cycloadditions of Substituted Furfuryl E-2-(Phenylsulfonyl)acrylates," Tetrahedron Lett. 1988, 29, 6059-6062. [pdf]

86. M. E. Jung and K. T. Hogan, "Chirality Transfer from Silicon to Carbon: Use of Optically Pure Cyclic Silanes with a Binaphthalene Chiral Unit," Tetrahedron Lett. 1988, 29, 6199-6202. [pdf]

87. M. E. Jung, R. B. Blum, B. J. Gaede, and M. R. Gisler, "Preparation and Diels-Alder Cycloadditions of Substituted Vinylene Carbonates (1,3-Dioxol-2-ones) and Related Compounds," Heterocycles 1989, 28, 93-97. [pdf]

88. M. E. Jung and S. M. Kaas, "Facile Synthesis of a Substituted Bicyclo[4.2.1]nonane via an Anionic [1,3]-Sigmatropic Shift: Use of Long Range 2D HETCOR and Difference NOE in Structure Determination," Tetrahedron Lett. 1989, 30, 641-644. [pdf]

89. M. E. Jung, W. D. Vaccaro, and K. R. Buszek, "Asymmetric Diels-Alder Reactions of Chiral Alkoxy Iminium Salts," Tetrahedron Lett. 1989, 30, 1893-1896. [pdf]

90. M. E. Jung and J. Gervay, "Solvent Effects in Intramolecular Diels-Alder Reactions of 2-Furfuryl Methyl Fumarates: Evidence for a Polar Transition State," J. Am. Chem. Soc. 1989, 111, 5469-5470. [pdf]

91. M. E. Jung, D. Jachiet, and J. C. Rohloff, "Facile Chemical Synthesis of S,S-Isodityrosine, A Naturally-Occurring Cross-Linking Amino Acid," Tetrahedron Lett. 1989, 30, 4211-4214. [pdf]

92. M. E. Jung and Y. H. Jung, "Rapid Synthesis of β-Hydroxy-α-amino Acids, such as L-Threonine, β-Hydroxyphenylalanine, and β-Hydroxyleucine, via an Application of the Sharpless Asymmetric Epoxidation," Tetrahedron Lett. 1989, 30, 6637-6640. [pdf]

93. M. E. Jung, I. D. Trifunovich, J. M. Gardiner, and G. L. Clevenger, "Preparation of Modified Nucleosides from Glucosamine: Rapid and Efficient Formal Total Synthesis of Several 2'-Deoxy C-Nucleosides," J. Chem. Soc., Chem. Commun. 1990, 84-85. [pdf]

94. M. E. Jung and W. Lew, "Diastereoselective Organocuprate Addition to Homochiral Ketals of 3-Acetylcyclopent-2-en-1-one," Tetrahedron Lett. 1990, 31, 623-626. [pdf]

95. M. E. Jung, "Substituent and Solvent Effects in Intramolecular Diels-Alder Reactions," Synlett 1990, 186-190. [pdf]

96. M. E. Jung and S J. Miller, "Preparation of N-Alkadienyl N-E-2-Arylethenylcarbamates via Sulfoxide Elimination in a Synthetic Approach to Lycorine," Heterocycles 1990, 30, 839-854. [pdf]

97. M. E. Jung and J. Gervay, "A New NMR Technique for Measuring the Ground State Populations of Formate Esters: Polar Aprotic Solvents Favor the s-cis (E)-Isomer of t-Butyl Formate," Tetrahedron Lett. 1990, 31, 4685-4688. [pdf]

98. M. E. Jung, Y. H. Jung, and Y. Miyazawa, "Facile Synthesis of Both Enantiomers of 2, 3, 4, 5, 6-Pentafluoro-
α-methoxybenzeneacetic Acid in High Optical Purity," Tetrahedron Lett.
1990, 31, 6983-6986. [pdf]

99. M. E. Jung and D. B. Head, "Synthesis of Fully Functionalized Intermediates for the Bottom Half of the 4-Acyloxymethyl Milbemycin Antibiotics,"
Bull. Soc. Chim. Fr. 1990, 830-834. [pdf]

100. M. E. Jung and J. Gervay, "Studies on the Gem-Dialkyl Effect in the Intramolecular Diels-Alder Reaction of 2-Furfuryl Methyl Fumarates: the Reactive Rotamer Effect, the Enthalpic Basis for the Acceleration, and Evidence For A Polar Transition State," J. Am. Chem. Soc. 1991, 113, 224-232. [pdf]

101. M. E. Jung and W. Lew, "Efficient Total Synthesis of the Cytotoxic Halogenated Monoterpene Aplysiapyranoid D," J. Org. Chem. 1991, 56, 1347-1349.
[pdf]

102. M. E. Jung and J. M. Gardiner, "Synthetic Approaches to 3'-Azido-3'-deoxythymidine and Other Modified Nucleosides," J. Org. Chem. 1991, 56, 2614-2615. [pdf]

103. M. E. Jung and A. Hagiwara, "New Alkene-forming Reaction: Phenanthrenes from 2-(2-Formylphenyl)benzaldehyde Bis-tosylhydrazone Decomposition," Tetrahedron Lett. 1991, 32, 3025-3028. [pdf]

104. M. E. Jung, C. Castro, and J. M. Gardiner, "Rapid Synthesis of 2',3'-Dideoxycytidine (ddC) from a Simple Achiral Precursor," Tetrahedron Lett. 1991, 32, 5717-5720. [pdf]

105. M. E. Jung and C. N. Zimmerman, "New Synthesis of Methyl 1,3-Butadiene-2-carboxylate by the Cheletropic Extrusion of Carbon Monoxide from 3-Carbomethoxy-3,4-pentadienal and a Study of Its Dimerization To Give Dimethyl Mikanecate (Dimethyl 4-Ethenyl-1-cyclohexene-1,4-dicarboxylate)," J. Am. Chem. Soc. 1991, 113, 7813-7814. [pdf]

106. M. E. Jung and G. L. Clevenger, "Conversion of D-Mannose into 1,5-Anhydro-D-Allitol-4,6-acetonide; Unusual Intramolecular Epoxy Alcohol Opening in Base," Tetrahedron Lett. 1991, 32, 6089-6092. [pdf]

107. M. E. Jung, "Stabilized Nucleophiles with Electron Deficient Alkenes and Alkynes," Chapter 1.1, in Volume 4 of "Comprehensive Organic Synthesis," Pergamon Press, Oxford, 1991, pp 1-67. [pdf]

108. M. E. Jung and Y. M. Choi, "New Synthesis of 2-Azetines and 1-Azabutadienes and the Use of the Latter in Diels-Alder Reactions; Total Synthesis of (±) δ-Coniceine," J. Org. Chem. 1991, 56, 6729-6730. [pdf]

109. M. E. Jung and I. D. Trifunovich, "Efficient Synthesis of 2',3'-Dideoxynucleosides and 2',3'-Dideoxy C-Nucleosides from D-Glucosamine," Tetrahedron Lett. 1992, 33, 2921-2924. [pdf]

110. M. E. Jung and J. M. Gardiner, "Synthesis of Antiviral Nucleosides from Crotonaldehyde. Part 3. Total Synthesis of Didehydrodideoxythymidine (d4T)," Tetrahedron Lett. 1992, 33, 3841-3844. [pdf]

111. M. E. Jung, L. Zeng, T. Peng, H. Zeng, Y. Le, and J. Su, "Total Synthesis of Bao Gong Teng A, a Natural Antiglaucoma Compound," J. Org. Chem. 1992, 57, 3528-3530. [pdf]

112. M. E. Jung, I. D. Trifunovich, and N. Lensen, "Easy Preparation of a Cyclobutanone Ketal via a Radical Cyclization. The Gem-Dialkoxy Effect," Tetrahedron Lett. 1992, 33, 6719-6722. [pdf]

113. M. E. Jung, D. C. D'Amico, and W. Lew, "Efficient Total Synthesis of the Cytotoxic Halogenated Monoterpene Aplysiapyranoid A," Tetrahedron Lett. 1993, 34, 923-926. [pdf]

114. M. E. Jung and C. Castro, "New Approach to the Synthesis of β-2'-Deoxyribonucleosides: Intramolecular Vorbrüggen Coupling," J. Org. Chem. 1993, 58, 807-808. [pdf]

115. M. E. Jung and A. W. Sledeski, "Efficient Total Synthesis of Racemic and Optically Active Cyclobut-A and Simple Analogues," J. Chem. Soc., Chem. Commun. 1993, 589-591. [pdf]

116. M. E. Jung, I. D. Trifunovich, and A. W. Sledeski, "A Simple Technique to Distinguish Between C s and C 2 Diastereomeric Diols Derived from Chiral Substrates," Heterocycles 1993, 35, 273-282. [pdf]

117. M. E. Jung and A. Vidal Gomez, "Efficient Method for the Preparation of 2α, 3β -Dichloro-4,4,10-trimethyldecalin Systems as a Route for the Synthesis of Dichlorolissoclimide," Tetrahedron Lett. 1993, 34, 2891-2894. [pdf]

118. M. E. Jung and C. S. Siedem, "Efficient Synthesis of a Hexasubstituted Aromatic Ring via an Intramolecular Michael-Aldol Process: Preparation of a Late Tricyclic Intermediate for the Synthesis of Pseudopterosin A," J. Am. Chem. Soc. 1993, 115, 3822-3823. [pdf]

119. M. E. Jung and H. Rhee, "New Efficient Method for the Synthesis of the Antiviral Agent Carbovir," Tetrahedron Lett. 1993, 34, 4449-4452. [pdf]

120. M. E. Jung, C. N. Zimmerman, G. T. Lowen, and S. I. Khan, "Diastereocontrol in Intermolecular Diels-Alder Reactions of Allenic Lactones: Synthetic Approach to the Plaunols," Tetrahedron Lett. 1993, 34, 4453-4456. [pdf]

121. Y. Nagao, M. Takahashi, Y. Abe, T. Misono, and M. E. Jung, "Synthesis of 1,1-Dialkoxy Derivatives of 2,5-Diphenylsilacyclopent-3-ene and 2,5-Diphenylsilacyclopentane," Bull. Chem. Soc. Jpn. 1993, 66, 2294-2296. [pdf]

122. M. E. Jung and S. W. T. Choe, "Stereospecific Intramolecular Formyl Transfer via Radical Cyclization-Fragmentation: Preparation of Alkyl 2-Deoxy-2
α-formylglycopyranosides and Similar Compounds," Tetrahedron Lett. 1993, 34, 6247-6250. [pdf]

123. M. E. Jung and D. C. D'Amico, "Enantiospecific Synthesis of All Four Diastereomers of 2-Methyl-3-((trialkylsilyl)oxy)alkanals: Facile Preparation of Aldols by Non-Aldol Chemistry," J. Am. Chem. Soc. 1993, 115, 12208-12209. [pdf]

124. M. E. Jung and H. L. Rayle, "An Improved Synthesis of 4-Methylene-2-cyclohexen-1-one," Synth. Commun. 1994, 24, 197-199. [pdf]

125. M. E. Jung, C. H. Kim, and L. v. d. Bussche, "Vicarious Nucleophilic Aromatic Substitution via Trapping of an α-Ketosulfonium Ion Generated by a Pummerer-Type Rearrangement of 2-(Phenylsulfinyl)phenols: Preparation of Biaryls," J. Org. Chem. 1994, 59, 3248-3249. [pdf]

126. P. M. Harrington and M. E. Jung, "Stereoselective Bromination of a β-Ribofuranosyl Amide. Enantioselective Synthesis of (+)-Hydantocidin," Tetrahedron Lett.
1994, 35, 5145-5148. [pdf]

127. M. E. Jung and H. Rhee, "π -Allylpalladium Formation from Allylic Amines via N,N-Ditosylimides and N-Tosylamides: Efficient Synthesis of the Antiviral Agent Carbovir," J. Org. Chem.
1994, 59, 4719-4720. [pdf]

128. M. E. Jung and J. M. Gardiner, "Asymmetric Synthesis of Carbohydrates: Synthesis of 2-Deoxy-D- and 2-Deoxy-L-xylofuranosides from a Simple Achiral Precursor," Tetrahedron Lett.
1994, 35, 6755-6758. [pdf]

129. M. E. Jung and S. M. Dansereau, "Benzo[H
]-1,6-naphthyridine Synthesis via Intramolecular Diels-Alder Reactions of Aryl Oxazoles: Synthetic Approach to 2-Bromoleptoclinidinone," Heterocycles 1994, 39, 767-778. [pdf]

130. M. E. Jung, D. Jachiet, S. I. Khan, and C. Kim, "New Method for the Preparation of o
-Aryloxyphenols: Pummerer-Type Rearrangement of an o-Hydroxyaryl Sulfoxide," Tetrahedron Lett. 1995, 36, 361-364. [pdf]

131. M. E. Jung and S. W. T. Choe, "Total Synthesis of Cyclophellitol and (1R
,2S)-Cyclophellitol from D-Mannose," J. Org. Chem. 1995, 60, 3280-3281. [pdf]

132. M. E. Jung and Y. H. Jung, "Efficient Enantioselective Synthesis of (2R
,3S) Methyl β-Hydroxytyrosinate from Achiral Starting Materials," Synlett 1995, 563-564. [pdf]

133. M. E. Jung and D. C. D'Amico, "Stereospecific Rearrangement of Optically Active Tertiary Allylic Epoxides to Give Optically Active Quaternary Aldehydes: Synthesis of α-Alkyl Amino Aldehydes and Acids," J. Am. Chem. Soc.
1995, 117, 7379-7380. [pdf]

134. M. E. Jung and M. Kiankarimi, "Gem-Dialkoxy Effect in Radical Cyclizations to Produce Cyclopropane Derivatives: Unusual Oxidation of a Dialkoxyalkyl Radical," J. Org. Chem.
1995, 60, 7013-7014. [pdf]

135. M. E. Jung and L. S. Starkey, "New Preparation of o
-Aryloxyphenols via Cyclohexenone Oxides," Tetrahedron Lett. 1995, 36, 7363-7366. [pdf]

136. E. D. Murray, Jr., D. Kantoci, S. A. DeWind, A. E. Bigornia, D. C. D'Amico, J. G. King, Jr., T. Pham, B. H. Levine, M. E. Jung, and W. J. Wechter, "Endogenous Natriuretic Factors 3: Isolation and Characterization of Human Natriuretic Factors LLU-α, LLU-β1, and LLU-γ," Life Sci.
1995, 57, 2145-2161. [pdf]

137. M. E. Jung, Y.-M. Cho, and Y. H. Jung, "Facile Synthesis of Optically Active 2-Hydroxymethyl-4-methylenecyclohexanol. Total De Novo Synthesis of Carbocyclic Sugars," Tetrahedron Lett.
1996, 37, 3-6. [pdf]

138. M. E. Jung and T. Lazarova, "Preparation of (Phenylsulfinyl)phenols from Aryl Sulfinates: 'Thia-Fries Rearrangement'," Tetrahedron Lett.
1996, 37, 7-8. [pdf]

139. M. E. Jung and B. T. Vu, "Substituent Effects on Intramolecular Dipolar Cycloadditions: The Gem-Dicarboalkoxy Effect," Tetrahedron Lett.
1996, 37, 451-454. [pdf]

140. D. P. C. McGee, D. P. Sebesta, S. S. O'Rourke, R. L. Martinez, M. E. Jung, and W. A. Pieken, "Novel Nucleosides via Intramolecular Functionalization of 2,2'-Anhydrouridine Derivatives," Tetrahedron Lett.
1996, 37, 1995-1998. [pdf]

141. W. J. Wechter, D. Kantoci, E. D. Murray, Jr., D. C. D'Amico, M. E. Jung, and W.-H. Wang, "A New Endogenous Natriuretic Factors: LLU-α," Proc. Natl. Acad. Sci. U. S. A.
1996, 93, 6002-6007. [pdf]

142. M. E. Jung and B. T. Vu, "Complete Diastereocontrol in Intramolecular 1,3-Dipolar Cycloadditions of 2-Substituted 5-Hexenyl and 5-Heptenyl Nitrones: Application to the Synthesis of the β-Lactam Antibiotic 1β-Methylthienamycin," J. Org. Chem.
1996, 61, 4427-4433. [pdf]

143. M. E. Jung and C. J. Nichols, "Highly Stereoselective Synthesis of trans, trans-4-Aryl-2,3-oxetanedimerthanols: Preparation of Oxetanocin A Analogues," Tetrahedron Lett.
1996, 37, 7667-7670. [pdf]

144. W. J. Wechter, E. D. Murray, Jr., D. Kantoci, and M. E. Jung, "Characterization of two New Endogenous Natriuretic Factors,"
J. Am. Soc. Nephrology
1996, 7, A2867. [pdf]

145. Y. Nagao, N. Namiki, S. Sakamoto, and M. E. Jung, "Synthesis of 2,5-Dimethyl and 2,5-Diphenylsilacyclopentane Derivatives and Their Reactions," in "43rd Symposium on Organometallic Chemistry," Kinki Chemical Society, Osaka, Japan, 1996, Abstract PA 112, pp. 50-51. [pdf]

146. M. E. Jung and C. J. Nichols, "A Novel Tandem [1,2]-Brook/Retro-[1,6]-Brook Rearrangement of a 1-Trimethylsilyl-2,4-pentadien-1-ol Anion," J. Org. Chem.
1996, 61, 9065-9067. [pdf]

147. C. Giessner-Prettre, S. Hückel, J. Maddaluno, and M. E. Jung, "Molecular Mechanics/ Continuum Reaction Field/Quantum Mechanics Study of the Intramolecular Diels-Alder Reaction of 2-Furfuryl Derivatives," J. Org. Chem.
1997, 62, 1439-1448. [pdf]

148. M. E. Jung and T. I. Lazarova, "Efficient Synthesis of Selectively Protected L-Dopa Derivatives from L-Tyrosine via Reimer-Tiemann and Dakin Reactions," J. Org. Chem.
1997, 62, 1553-1555. [pdf]

149. Y. Nagao, K. Miyakawa, S. Sakamoto, M. Takahashi, Y. Abe, and M. E. Jung, "Synthesis of trans-1,1-dialkoxy-2,5-diphenyl-1-sila-3-cyclopentenes and their 2-alkyl derivatives," Nippon Kagaku Kaishi
1997, 213-218. [pdf]

150. M. E. Jung and K. L. Anderson, "Stereospecific Rearrangements of Optically Active 2-Aryl-3-Ethenyloxiranes to Give Optically Active β-Ethenylbenzeneethanols: Benzyl vs. Allyl Cations and an Efficient Synthesis of (S
)-Ibuprofen," Tetrahedron Lett. 1997, 38, 2605-2608. [pdf]

151. M. E. Jung and Y. Xu, "Efficient Syntheses of L-Ribose and 2-Deoxy L-Ribose from D-Ribose and L-Arabinose," Tetrahedron Lett.
1997, 38, 4199-4202. [pdf]

152. M. E. Jung and L. S. Starkey, "Total Synthesis of S,S-Isodityrosine," Tetrahedron
1997, 53, 8815-8824. [pdf]

153. M. E. Jung and H. L. Rayle, "Generation of [5.5.n]Tricyclic Ring Systems by Radical Promoted Inter- and Intramolecular [3 + 2] Cycloadditions," J. Org. Chem.
1997, 62, 4601-4609. [pdf]

154. M. E. Jung and R. Marquez, "Gem-Disubstituent Effects in Small Ring Formation: Novel Ketal Ring Size Effect," Tetrahedron Lett.
1997, 38, 6521-6524. [pdf]

155. M. E. Jung and M. H. Parker, "Synthesis of Several Naturally Occurring Polyhalogenated Monoterpenes of the Halomon Class," J. Org. Chem.
1997, 62, 7094-7095. [pdf]

156. M. E. Jung and D. C. D'Amico, "Stereospecific Formation of Optically Active 2-([Trialkylsilyloxy]methyl)tetrahydrofuran-3-ols via Diastereoselective Epoxidation and Rearrangement of 5-[(Trialkylsilyl)oxy]-2-alken-1-ols," J. Am. Chem. Soc.
1997, 119, 12150-12158. [pdf]

157. M. E. Jung and T. W. Johnson, "Total Synthesis of 7-Deoxyxestobergsterol A, a Novel Pentacyclic Steroid of the Xestobergsterol Class," J. Am. Chem. Soc.
1997, 119, 12412-12413. [pdf]

158. M. E. Jung and S. Angelica, "An Intramolecular Prins Double Cyclization Catalyzed By Silyl Triflates," J. Org. Chem.
1997, 62, 9182-9187. [pdf]

159. M. E. Jung and C. J. Nichols, "Synthesis of Methylene-Expanded Oxetanocin Isonucleosides in Both Enantiomeric Forms," J. Org. Chem.
1998, 63, 347-355. [pdf]

160. M. E. Jung and Y. Xu, "Efficient Synthesis of Specifically Deuterated Nucleosides: Preparation of 4'-Deuteriothymidine," Heterocycles
1998, 47, 349-356. [pdf]

161. M. E. Jung and M. Kiankarimi, "Substituent and Solvent Effects in the Intramolecular Diels-Alder Reaction of 6-Furyl Hexenoates," J. Org. Chem.
1998, 63, 2968-2974. [pdf]

162. M. E. Jung and O. Kretschik, "Enantiospecific Total Synthesis of L-2',3'-Dideoxy Isonucleosides via Regioselective Opening of Optically Active C2-Symmetric 1,4-Pentadiene bis-Epoxide," J. Org. Chem.
1998, 63, 2975-2981. [pdf]

163. M. E. Jung and B. T. Fahr, "Total Synthesis of the Cytotoxic Marine Natural Product, Aplysiapyranoid C," J. Org. Chem.
1998, 63, 2982-2987. [pdf]

164. M. E. Jung and C. J. Nichols, "A de novo Synthesis of Ethyl 2-Deoxy-L-ribosides," Tetrahedron Lett.
1998, 39, 4615-4618. [pdf]

165. M. E. Jung, C. Castro, and S. I. Khan, "Novel Lewis Acid-Catalyzed Rearrangement of a Sugar-Base Hybrid to Afford an Anhydronucleoside," Nucleosides Nucleotides
1998, 17, 2383-2387. [pdf]

166. M. E. Jung and M. Kiankarimi, "Synthesis of Methylene-Expanded 2',3'-Dideoxyribonucleosides," J. Org. Chem.
1998, 63, 8133-8144. [pdf]

167. M. E. Jung, U. Karama, and R. Marquez, "Conversion of Homoallylic Alcohols with Alkene Protection to the Corresponding Methyl Ketones," J. Org. Chem.
1999, 64, 663-665. [pdf]

168. M. E. Jung, R. Marquez, and K. N. Houk, "Prediction of Variations in Efficiencies of 4-Exo Trig Radical Cyclizations," Tetrahedron Lett.
1999, 40, 2661-2664. [pdf]

169. M. E. Jung and R. Marquez, "Rearrangement of Epoxides in Non-aldol Aldol Process: Allylic vs. Tertiary and Secondary Carbocationic Centers," Tetrahedron Lett.
1999, 40, 3129-3132. [pdf]

170. M. E. Jung and N. Nishimura, "Stereoselective Formation of Formal Exo Diels-Alder Adducts of Silyloxydienes and Allenecarboxylates," J. Am. Chem. Soc.
1999, 121, 3529-3530. [pdf]

171. M. E. Jung and T. I. Lazarova, "New Efficient Method for the Total Synthesis of (S
,S)-Isodityrosine from Natural Amino Acids," J. Org. Chem. 1999, 64, 2976-2977. [pdf]

172. M. E. Jung, "New Gem- and Vic-Disubstituent Effects on Cyclizations," Synlett
1999, 843-846. [pdf]

173. M. E. Jung, C. J. Nichols, O. Kretschik, and Y. Xu, "Synthesis and Testing of New Modified Nucleosides," Nucleosides Nucleotides
1999, 19, 541-6. [pdf]

174. M. E. Jung, W. S. Lee, and D. Sun, "Extension of Non-aldol Aldol Process to Bis(propionates): Synthesis of Four Diastereomeric 3,5-Dialkoxy-2,4-dimethylalkanals,"Org. Lett.
1999, 1, 307-309. [pdf]

175. M. E. Jung and J. Pontillo, "Facile Preparation of Allenic Hydroxyketones via Rearrangement of Propargylic Alcohols," Org. Lett.
1999, 1, 367-369. [pdf]

176. A. D. Watson, G. Subbanagounder, D. S. Welsbie, K. F. Faull, M. Navab, M. E. Jung, A. M. Fogelman, and J. A. Berliner, "Structural Identification of a Novel Pro-inflammatory Epoxy Isoprostane Phospholipid in Mildly Oxidized Low Density Lipoprotein," J. Biol. Chem.
1999, 274, 24787-24798. [pdf]

177. M. E. Jung and J. M. MacDougall, "First Enantioselective Total Synthesis of the Endogenous Natriuretic Agent LLU-α," Tetrahedron Lett.
1999, 40, 6339-6342. [pdf]

178. M. E. Jung, W. Mengel, and T. L. Newton, "A Short, Convenient Synthesis of 2-Aryl-3,3-disubstituted Glycidic Esters via Organometallic Addition to α-Bromopyruvates," Synth. Commun.
1999, 29, 3659-3666. [pdf]

179. M. E. Jung, E. C. Yang, B. T. Vu, M. Kiankarimi, E. Spyrou, and J. Kaunitz, "Glycosylation of Fluoroquinolones Through Direct and Oxygenated Polymethylene Linkages as a Sugar-Mediated Active Transport System for Antimicrobials," J. Med. Chem.
1999, 42, 3899-3909. [pdf]

180. M. E. Jung and T. W. Johnson, "Unusual Cyclization Products Derived from Photolysis of Breslow's Steroidal Benzophenone Esters," J. Org. Chem.
1999, 64, 7651-7653. [pdf]

181. M. E. Jung and U. Karama, "Highly Diastereoselective Markovnikov Hydration of 3,4-Dialkoxy-1-alkenes and 4,5-Dialkoxy-2-alkenes via a Hydroboration-Oxidation Process," Tetrahedron Lett.
1999, 40, 7907-7910. [pdf]

182. M. E. Jung and Y. Xu, "Efficient Synthesis of 2-Deoxy L-Ribose from L-Arabinose: Mechanistic Information on the 1,2-Acyloxy Shift in Alkyl Radicals," Org. Lett.
1999, 1, 1517-1519. [pdf]

183. M. E. Jung and T. W. Johnson, "First Total Synthesis of Xestobergsterol A and Active Structural Analogues of the Xestobergsterols," Org. Lett.
1999, 1, 1671-1674. [pdf]

184. M. E. Jung and D. Sun, "Stereoselective Production of β-Amino Alcohols and β-Thioacyl Alcohols via an Application of the non-Aldol Aldol Process," Tetrahedron Lett.
1999, 40, 8343-8346. [pdf]

185. C. Castro, C. Chen, and M. E. Jung, "Intramolecular Glycosylation to form 2,6-Dioxo-4-methoxypyrimidine Nucleosides via O6,5'-Cyclonucleosides," Nucleosides Nucleotides
1999, 18, 2415-2423. [pdf]

186. H. Rhee, D.-O. Yoon, and M. E. Jung, "Efficient Synthesis of the Carbocyclic Nucleoside, (±)-Homocarbovir via Allylpalladium Complex Formation from an Allyl N
,N-Ditosylimide Substrate," Nucleosides Nucleotides 2000, 19, 619-628. [pdf]

187. A. S. Fraser, A. M. Kawasaki, M. E. Jung, and M. Manoharan, "An Efficient Method for the Synthesis of 2'-O-Modified Nucleosides Via Double Alkylation using Cyclic Sulfates," Tetrahedron Lett.
2000, 41, 1523-1526. [pdf]

188. M. E. Jung and B. T. Fahr, "Novel Base-Induced [1,2]-Acyl Shift of Allylic Esters of Cyclopropane Carboxylic Acids," J. Org. Chem.
2000, 65, 2239-2242. [pdf]

189. M. E. Jung and A. Toyota, "Efficient Synthesis of Several Methylene-Expanded Oxetanocin Nucleoside Analogues," Tetrahedron Lett.
2000, 41, 3577-3581. [pdf]

190. M. E. Jung and R. Marquez, "Efficient Synthesis of the C1-C11 Fragment of the Tedanolides. The Non-aldol Aldol Process in Synthesis," Org. Lett.
2000, 2, 1669-1672. [pdf]

191. M. E. Jung, A. Huang, and T. W. Johnson, "Unusual Diastereoselectivity in Intramolecular Diels-Alder Reactions of Substituted 3,5-Hexadienyl Acrylates. Preference for a Boat-like Structure of the Six-Atom Tether due to Ester Overlap," Org. Lett.
2000, 2, 1835-1837. [pdf]

192. M. E. Jung and A. Huang, "Use of Optically Active Cyclic N
,N-Dialkyl Aminals in Asymmetric Induction, " Org. Lett. 2000, 2, 2659-2661. [pdf]

193. Y. Nagao, S. Sakamoto, K. Miyakawa, Y. Abe, and M. E. Jung, "Synthesis of 1-substituted derivatives of 2,5-diphenylsilacyclopent-3-enes and 2,5-diphenylsila-cyclopentanes," Nippon Kagaku Kaishi
2000, 411-417. [pdf]

194. S. W. T. Choe and M. E. Jung, "Preparation of Various C-2 Branched Carbohydrates Using Stereospecific Intramolecular Radical Reactions," Carbohydr. Res.
2000, 329, 731-744. [pdf]

195. M. E. Jung and C. P. Lee, "Use of the Non-Aldol Aldol Process in the Synthesis of the C1-C11 Fragment of the Tedanolides: Use of Lactol Ethers in Place of Tetrahydrofurans," Tetrahedron Lett.
2000, 41, 9719-9723. [pdf]

196. M. E. Jung and B. S. Lee, "Unusual α-Methylation of Alkoxyaryl Ketones with Higher Order Methyl Cuprate and Lithium Bromide," J. Org. Chem.
2000, 65, 9241-9244. [pdf]

197. M. E. Jung and C. P. Lee, "Synthesis of a Fully Functionalized Protected C1-C11 Fragment for the Synthesis of the Tedanolides," Org. Lett.
2001, 3, 333-336. [pdf]

198. M. E. Jung and T. W. Johnson, "First Total Synthesis of Xestobergsterol A and Active Structural Analogues of the Xestobergsterols," Tetrahedron
2001, 57, 1449-1481. [pdf]

199. H. Cai, J. Strouse, D. Dumlao, M. E. Jung, and S. Clarke, "Distinct Reactions Catalyzed by Bacterial and Yeast trans-Aconitate Methyltransferases," Biochemistry
2001, 40, 2210-2219. [pdf]

200. M. E. Jung and P. Davidov, "First Conclusive Evidence of the Trapping of Primary Ozonides," Org. Lett.
2001, 3, 627-629. [pdf]

201. D. J. Tantillo, K. N. Houk, and M. E. Jung, "Origins of Stereoselectivity in Intramolecular Diels-Alder Cycloadditions of Dienes and Dienophiles Linked by Ester and Amide Tethers," J. Org. Chem.
2001, 66, 1938-1940. [pdf]

202. M. E. Jung and A. Toyota, "Preparation of 4'-Substituted Nucleosides by Substitution of the Nucleoside 5'-Esters," J. Org. Chem.
2001, 66, 2624-2635. [pdf]

203. M. E. Jung and N. Nishimura, "Enantioselective Formal Total Synthesis of (-)-Dysidiolide," Org. Lett.
2001, 3, 2113-2115. [pdf]

204. M. E. Jung and F. Slowinski, "Rhodium-Catalyzed Decomposition of Indole-Substituted α-Diazo-β-Keto Esters: Three Different Reactions Based on Indole Oxidation State," Tetrahedron Lett.
2001, 42, 6835-6838. [pdf]

205. M. E. Jung and P. Davidov, "The First Reported Anionic Retro-Ene Reaction," Org. Lett.
2001, 3, 3025-3027. [pdf]

206. M. E. Jung, A. Toyota, E. De Clercq, and J. Balzarini, "Synthesis and Biological Activity of a Series of Methylene-Expanded Oxetanocin Nucleoside Analogues," Monatshefte Chem.
2002, 133, 499-520. [pdf]

207. M. E. Jung and G. Piizzi, "Novel Rearrangements of 4-Silyl-3-buten-2-ones,"J. Org. Chem.
2002, 67, 3911-3914. [pdf]

208. M. E. Jung and J. Pontillo, "Synthetic Approach to Analogues of the Original Structure of Sclerophytin A," J. Org. Chem.
2002, 67, 6848-6851. [pdf]

209. M. E. Jung and P. D. Davidov, "Efficient Synthesis of a Tricyclic BCD Analogue of Ouabain: Lewis Acid Catalyzed Diels-Alder Reactions of Sterically Hindered Systems," Angew. Chem. Int. Ed.
2002, 41, 4125-4128. [pdf]

210. M. E. Jung and A. van den Heuvel, "Diastereoselectivity in non-Aldol Aldol Reactions: Silyl Triflate Promoted Payne Rearrangements," Tetrahedron Lett.
2002, 43, 8169-8172. [pdf]

211. M. E. Jung, A. Kers, G. Subbanagounder, and J. A. Berliner, "Endothelial Activation by an Epoxy Isoprostane Phsopholipid. Total Synthesis of Epoxy Isoprostanes," Chem Commun.
2003, 196-197. [pdf]

212. M. E. Jung and G. Piizzi, "Synthesis of the A/B Ring System of Ouabain," Org. Lett.
2003 5, 137-140. [pdf]

213. A. G. Leach, R. Wang, G. E. Wohlhieter, S. I. Khan, M. E. Jung, and K. N. Houk, "Theoretical Elucidation of Kinetic and Thermodynamic Control of Radical Addition Regioselectivity," J. Am. Chem. Soc.
2003, 125, 4271-4278. [pdf]

214. M. E. Jung and G. Piizzi, "Synthetic Approach to the AB Ring System of Ouabain," J. Org. Chem.
2003, 68, 2572-2582. [pdf]

215. M. E. Jung and J. Pontillo, "Synthetic Approach to Analogues of Sclerophytin A," Tetrahedron
2003, 59, 2729-2736. [pdf]

216. M. E. Jung, B. Hoffmann, B. Rausch, and J.-M. Contreras, “Use of Hindered Silyl Ethers as Protecting Groups for the Non-Aldol Aldol Process,” Org. Lett.
2003, 5, 3159-3161. [pdf]

217. K. M. Connolly, B. M. Smith, R. Pilpa, U. Ilangovan, M. E. Jung, and R. T. Clubb, “Sortase from S. aureus
Does not Contain a Thiolate-imidazolium Ion Pair in its Active Site,” J. Biol. Chem. 2003, 278, 34061-34065. [pdf]

218. M. E. Jung, A. van den Heuvel, A. G. Leach, and K. N. Houk, “Unexpected Syn Hydride Migration in the Non-aldol Aldol Reaction,”Org. Lett.
2003, 5, 3375-3378. [pdf]

219. M. E. Jung and J. I. Wasserman, “Efficient Synthesis of Vinyl Chlorides and/or gem
-Dichlorides from Ketones by Treatment with Tungsten Hexachloride,” Tetrahedron Lett. 2003, 44, 7273-7275. [pdf]

220. M. E. Jung and A. van den Heuvel, "Tandem non-Aldol Aldol-Mukaiyama Aldol Process: Synthesis of Bis-(β-Silyloxy)ketones," Org. Lett
2003, 5, 4705-4707. [pdf]

221. M. E. Jung and B. A. Duclos, "Diastereoselectivity in the Carroll Rearrangement of β-Keto Esters of Tertiary Allylic Alcohols," Tetrahedron Lett.
2004, 45, 107-109. [pdf]

222. J. E. Katz, D. S. Dumlao, J. I. Wasserman, M. G. Lansdown, M. E. Jung, K. F. Faull and S. Clarke, "3-Isopropylmalate is the Major Endogenous Substrate of the Saccharomyces cerevisiae trans-Aconitate Methyltransferase," Biochemistry
2004, 43, 5976-5986. [pdf]

223. M. E. Jung and A. Maderna, "Allylation of Acetals and Ketals with Allyltrimethylsilane Catalyzed by the Mixed Lewis Acid System AlBr3 /CuBr," Tetrahedron Lett. 2004, 45, 5301-5304. [pdf]

224. C. K. Liew, B. T. Smith, R. Pilpa, U. Ilangovan, K. M. Connolly, M. E. Jung, and R. T. Clubb, "Localization and mutagenesis of the sorting signal binding site on sortase A from Staphylococcus aureus,"FEBS Lett. 2004
, 571, 221-226. [pdf]

225. M. E. Jung and S.-J. Min, "Novel Formation of a Bridged Bicyclic Furan by Rearrangement of a Tetrahydroxydecalinone," Tetrahedron Lett.
2004, 45, 6753-6755. [pdf]

226. M. E. Jung and A. Maderna, "Microwave-assisted Allylation of Acetals with Allyltrimethylsilane in the Presence of CuBr," J. Org. Chem. 2004
69, 7755-7757. [pdf]

227. Y. Nagao, C. Kimura, K. Kozawa, and M. E. Jung,"Synthesis, Stereochemistry, and Reactions of 2,5-Diphenylsilacyclopentenes," Silicon Chem. 2003, 2, 99-107. [pdf]

228. M. E. Jung, S.-J. Min, K. N. Houk, and D. Ess, "Synthesis and Relative Stability of 3,5-Diacyl 4,5-Dihydro-1H-Pyrazoles Prepared by Dipolar Cycloaddition of Enones and α -Diazoketones," J. Org. Chem. 2004
, 69, 9085-9089. [pdf]

229. M. E. Jung, D. Ho, and H. V. Chu, "Synthesis of Highly Substituted Cyclohexenes via Mixed Lewis Acid-Catalyzed Diels-Alder Reactions of Highly Substituted Dienes and Dienophiles," Org. Lett.
2005, 7, 1645-1651. [pdf]

230. M. E. Jung and G. Piizzi, "Gem-Disubstituent Effect: Theoretical Basis and Synthetic Applications," Chem. Rev. 2005
, 105, 1735-1766. [pdf]

231. M. E. Jung and A. Maderna, "Synthesis of Bicyclo[2.2.2]oct-5-en-2-ones via a Tandem Intermolecular Michael Addition Intramolecular Aldol Process (a Bridged Robinson Annulation)," Tetrahedron Lett. 2005
, 46, 5057-5061.[pdf]

232. M. E. Jung and S.-J. Min, "Intramolecular Diels-Alder Reactions of Optically Active Allenic Ketones: Chirality Transfer in the Preparation of Substituted Oxa-bridged Octalones," J. Am. Chem. Soc. 2005
, 127, 10834-10835.[pdf]

233. M. E. Jung, N. Nishimura, and A. R. Novack, "Versatile Diastereoselectivity in Formal [3,3]-Sigmatropic Shifts of Substituted 1-Alkenyl-3-alkylidenecyclobutanols and Their Silyl Ethers," J. Am. Chem. Soc. 2005, 127, 11206-11207.[pdf]

234. Y. Akiba, M. E. Jung, S. Ouk, and J. D. Kaunitz, "A Novel Small Molecule CFTR Inhibitor Attenuates HCO3 Secretion And Duodenal Ulcer Formation In Rats" Amer. J. Physiol. GI Liver Physiol. 2005 , 289, G753-G759.[pdf]

235. J. A. Richardson, C. M. Amantea, K. Nguyen, M. E. Jung, T. J. Hahn, and F. Parhami, "Characterization of Osteogenic Oxysterols and their Molecular Mechanism(s) of Action," J. Bone Mineral Res. 2005, 20, Abstract M427, S414-S415. [pdf]

236. M. E. Jung, J. A. Berliner, D. Angst, D. Yue, L. Koroniak, A. D. Watson, and R. Li, "Total Synthesis of the Epoxy Isoprostane Phospholipids PEIPC and PECPC," Org. Lett. 2005, 7, 3933-3935. [pdf]

237. M. E. Jung and A. R. Novack, "Formation of 3,4-Dimethyl-2-pyrones from Allene Carboxylates and 2-Silyloxydienes via 3-Carboethoxyethylidene Cyclobutanols" Tetrahedron Lett. 2005, 46, 8237-8240.[pdf]

238. M. E. Jung, J. J. Clemens, N. Suttee, C. K. Liew, and R. T. Clubb, "Synthesis of (2R, 3S) 3-Amino-4-mercapto-2-butanol, a Threonine Analogue for Covalent Inhibition of Sortases," Bioorg. Med. Chem. Letts. 2005, 15, 5076-5079. [pdf]

239. M. E. Jung and W.-J. Kim, "Practical Syntheses of Dyes for Difference Gel Electrophoresis (DIGE)," Bioorg. Med. Chem. 2006, 14, 92-97. [pdf]

240. M. T. Naik, N. Suree, N. U. Ilangovan, C. K. Liew, J. Clemens, M. E. Jung, and R. T. Clubb, "A Calcium Modulated Loop Closure Mechanism Activates Cell Surface Protein Anchoring by the Staphylococcus aureus Sortase A Transpeptidase," J. Biol. Chem. 2006, 281, 1817-182642. [pdf]

241. Y.-L. Zhao, C. P. Suhrada, M. E. Jung and K. N. Houk, "The 3-Vinylmethylenecyclobutane–4-Methylenecyclohexene Rearrangement: Theoretical Investigation of a Stereoselective Stepwise Cope Rearrangement," J. Am. Chem. Soc. 2006, 128, 11106-11113. [pdf]

242. M. E. Jung and B. A. Duclos, "Synthetic Approach to Analogues of Betulinic Acid," Tetrahedron 2006, 62, 9321-9334. [pdf]

243. M. E. Jung and M. Murakami, "Total Synthesis of (±)-Hedychenone: Trimethyldecalin Terpenes via Stepwise Allenoate Diene Cycloaddition,"
Org. Lett. 2006, 8, 5857-59. [pdf]

244. M. E. Jung and D. G. Ho, "Stepwise Acid-Promoted Double-Michael Process: an Alternative to Diels-Alder Cycloadditions for Hindered Silyloxydiene-Dienophile Pairs,"
Org. Lett. 2007, 9, 375-378. [pdf]

245. M. E. Jung and M. Murakami, "Total Synthesis of (±)-Hedychilactone B: Stepwise Allenoate Diene Cycloaddition to Prepare Trimethyldecalin Systems," Org. Lett. 2007, 9, 461-463. [pdf]

246. M. E. Jung and S.-J. Min, "Approaches to the Synthesis of Arisugacin A," Tetrahedron 2007, 63, 3682-3701. [pdf]

247. M. C. Duncan, D. G. Ho, J. Huang, M. E. Jung, and G. S. Payne, "Composite Synthetic Lethal Identification of Membrane Traffic Inhibitors," Proc. Natl. Acad. Sci. U. S. A. 2007, 104, 6235-6240. [pdf]

248. J. M. Tsay, M. Trzoss, L. Shi, X. Kong, M. Selke, M. E. Jung, and S. Weiss, "Singlet Oxygen Production by Peptide-Coated Quantum Dot-Photosensitizer Conjugates," J. Am. Chem. Soc. 2007, 129, 36865-6871. [pdf]

249. N. Suree, M. E. Jung, and R. T. Clubb, "Recent Advances Towards New Anti-infective Agents that Inhibit Cell Surface Protein Anchoring in Staphylococcus aureus and Other Gram-positive Pathogens," Mini Reviews in Medicinal Chemistry 2007, 7, 991-1000. [pdf]

250. M. E. Jung and D. Yoo, "Synthesis of the C
1 -C12 Fragment of the Tedanolides. Aldol-Non-Aldol Aldol Approach," Org. Lett. 2007, 9, 3543-3546. [pdf]

251. M. E. Jung and D. Yoo, "Unprecedented Rearrangement of a 4-Alkoxy-5-bromoalk-2-en-1-ol to a Cyclopentenone via an Iso-Nazarov Cyclization Process," J. Org. Chem. 2007, 72, 8565-8568. [pdf]

252. M. E. Jung and J. M. Murphy, "Functional Group Selectivity in Reactions of Epoxides with Tungsten Hexachloride," Tetrahedron Lett. 2007, 48, 8388-8391.[pdf]

253. M. E. Jung and T.-H. Zhang, "New Protocol for Anti-Selective Aldol Condensation of Ethyl Ketones with
α-Alkoxyaldehydes," Org. Lett. 2008, 10, 1371-40. [pdf]

254. M. E. Jung and D. Yoo, "Synthesis of the C
1 -C12 Fragment of the Tedanolides. Selective Hydroboration-protonation of Allylic Alcohol Approach," Tetrahedron Lett. 2008, 49, 816-819. [pdf]

255. W. Zhang, K. Watanabe, X. Cai, M. E. Jung, Y. Tang, and J. Zhan, "Identifying the Minimal Enzymes Required for Anhydrotetracycline Biosynthesis,"
J. Am. Chem. Soc. 2008, 130, 6068-6069. [pdf]

256. M. E. Jung and D. A. Allen, "Facile Synthesis of syn 2-Alkyl-3-trialkylsilyloxycycloalkanones via the First Non-Aldol Aldol Process of 2,3-Epoxycycloalkanols," Org. Lett. 2008, 10, 2039-2041. [pdf]

257. M. E. Jung and G-Y. Im, "Convergent Total Synthesis of the Racemic HIF-1 Inhibitor Laurenditerpenol,"
Tetrahedron Lett. 2008, 49, 4962-4964. [pdf]

258. M. E. Jung and H. V. Chu, "Preparation of a Functionalized Tetracyclic Intermediate for the Synthesis of Rhodexin A," Org. Lett. 2008, 10, 3647-3649. [pdf]

259. M. E. Jung, J. A. Berliner, L. Koroniak, A. D. Watson, and B. G. Gugiu, "Improved Synthesis of the Epoxy Isoprostane Phospholipid PEIPC and its Reactivity with Amines," Org. Lett. 2008, 10, 4207-4209. [pdf]

260. M. E. Jung and D. A. Allen, "Use of 4-Cyanocoumarins as Dienophiles in a Facile Synthesis of Highly Substituted Dibenzopyranones," Org. Lett. 2009, 11, 757-760.[pdf]

261. M. E. Jung and F. Perez, "Synthesis of 2-Substituted 7-Hydroxybenzofuran-4-carboxylates via Addition of Silyl Enol Ethers to o-Benzoquinone Esters," Org. Lett. 2009, 11, 2165-67. [pdf]

262. C. Tran, S. Ouk, N. J. Clegg, Y. Chen, P. A. Watson, V. Arora, J. Wongvipat, P. M. Smith-Jones, D. Yoo, A. Kwon, T. Wasielewska, D. Welsbie, C. Chen, C. S. Higano, T. M. Beer, D. T. Hung, H. I. Scher, M. E. Jung, and C. Sawyers, "Development of a Second-Generation Antiandrogen for Treatment of Advanced Prostate Cancer," Science 2009, 324, 787-790. [pdf]

263. M. E. Jung, J. Cordova, and M. Murakami, "Total Synthesis of (±)-Kellermanoldione: Stepwise Cycloaddition of a Functionalized Diene and Allenoate," Org. Lett. 2009, 11, 3882-3885. [pdf]

264. N. Suree, C. K. Liew, V. Villareal, W. Thieu, E. A. Fadeev, J. J. Clemens, M. E. Jung and R. T. Clubb, "The Structure of the Staphylococcus aureus Sortase-Substrate Complex Reveals How the Universally Conserved LPXTG Sorting Signal is Recognized," J. Biol. Chem. 2009, 284, 24465-24477. [pdf]

265. L. Du, R. Damoiseaux, S. Nahas, J. Pollard, J. Goldstine, H. Hu, M. E. Jung, R. A. Gatti, "Identification of compounds with the ability to induce readthrough of nonsense mutations," J. Experimental Med. 2009, 206, 2285-2297. [pdf]

266. N. Suree, S. W. Yi, W. Thieu, M. Marohn, R. Damoiseaux, A. Chan, M. E. Jung and R. T. Clubb, "Discovery and Structure Activity Relationship Analysis of Staphylococcus aureus Sortase A Inhibitors," Bioorg. Med. Chem. 2009, 7174-7185. [pdf]

267. M. E. Jung and R. Salehi-Rad, "Total Synthesis of Auripyrone A Using a Tandem Non-Aldol Aldol-Paterson Aldol Process as a Key Step," Angew. Chem. 2009 48, 8766-8769. [pdf]

268. M. E. Jung and G-Y. Im, "The Total Synthesis of Racemic Laurenditerpenol, an HIF-1 Inhibitor," J. Org. Chem. 2009, 74, 8739-8753. [pdf]

269. M. C. Wolf, A. N. Freiberg, T.-H. Zhang, Z. Akyol-Ataman, A. Grock, P. W. Hong, J. Li, N. F. Watson, A. Q. Fang, H. C. Aguilar, M. Porotto, A. N. Honko, R. Damoiseaux, J. P. Miller, S. E. Woodson, S. Chantasirivisal, V. Fontanes, O. A. Negrete, P. Krogstad, A. Dasgupta, A. Moscona, L. E. Hensley, S. P. Whenlan, K. F. Faull, M. R. Holbrook, M. E. Jung, and B. Lee, "A Broad-spectrum Antiviral Targeting Entry of Enveloped Viruses," Proceedings of the National Academy of Sciences of the United States of America (PNAS) 2010, 107, 3157-62. [pdf]

270. M. E. Jung, S. Ouk, D. Yoo, C. L. Sawyers, C. Chen, C. Tran, and J. Wongvipat, "Structure-Activity Relationship for Thiohydantoin Androgen Receptor Antagonists for Castration-Resistant Prostate Cancer (CRPC)," J. Med. Chem. 2010, 53, 2779-2796. [pdf]

271. J. S. Johnson, V. Meliton, W. K. Kim, K. B. Lee, J. C. Wang, K. Nguyen, D. Yoo, M. E. Jung, E. Atti, S. Tetradis, R. C. Pereira, T. J. Hahn, F. Farouz, S. Thies and F. Parhami, "Novel Osteogenic Oxysterols Induce Osteogenic and Inhibit Adipogenic Differentiation of Marrow Stromal Cells In Vitro and Stimulate Bone Formation and Spinal Fusion In Vivo," Am. Soc. Bone Mineral Res. 2010, Abstract 210. [pdf]

272. M. E. Jung, M. Chaumontet, and R. Salehi-Rad, "Total Synthesis of Auripyrone B Using a Non-Aldol Aldol-Cuprate Opening Process," Org. Lett. 2010, 12, 2872-2875. [pdf]

273. M. E. Jung and J. J. Chang, "Enantiospecific Formal Total Synthesis of (+)-Fawcettimine," Org. Lett. 2010, 12, 2962-2965. [pdf]

274. M. Aghajan, N. Jonai, F. Fu, K. Flick, M. Luo, X. Cai, I. Ouni, N. Pierce, R. Hao, B. Lomenick, R. Damoiseaux, R. Verma, Y. Li, C. Li, K. N. Houk, M. E. Jung, L. Huang, R. J. Deshaies, P. Kaiser, and J. Huang, "Chemical Genetics of TOR Identifies an SCF Family E3 Ubiquitin Ligase Inhibtior," Nature Biotechnology 2010, 28, 738-742. [pdf]

275. M. E. Jung and R. Salehi-Rad, "Dipyrone Approach toward the Synthesis of the Cytotoxic Natural Product Auripyrone A," Tetrahedron Lett. 2010, 50, 4931-4933. [pdf]

276. W. Xu, X. Cai, M. E. Jung, and Y. Tang, "Analysis of Intact and Dissected Fungal Polyketide Synthase-Nonribosomal Peptide Synthetase in vitro and in Saccharomyces cerevisiae," J. Am. Chem. Soc. 2010, 132, 13604-13607. [pdf]

277. M. E. Jung, T.-H. Zhang, R. M. Lui, O. Gutierrez, and K. N. Houk, "Synthesis of a trans, syn, trans Dodecahydrophenanthrene via a Bicyclic Transannular Diels-Alder (BTADA) Reaction: Intermediate for the Synthesis of Fusidic Acid," J. Org. Chem. 2010, 75, 6933-6940. [pdf]

278. M. E. Jung and R. M. Lui, "Studies toward the Syntheses of Cucurbitacins B and D," J. Org. Chem. 2010, 75, 7146-7158. [pdf]

279. F. Vigant, M. E. Jung, and B. Lee, "Positive Reinforcement for Viruses," Chem. Biol. 2010, 17, 1049-1051. [pdf]

280. M. E. Jung and T. A. Dong, "Improved Synthesis of 4-Amino-7-nitrobenz-2,1,3-oxadiazoles using NBD Fluoride," Tetrahedron Lett. 2011, 52, 2533-2535. [pdf]

281. J. Johnson, V. Meliton, W. K. Kim, K. B. Lee, J. Wang, K. L. Nguyen, D. Yoo, M. E. Jung, E. Atti, S. Tetradis, R. Pereira, C. Magyar, T. Nargizyan, T. Hahn, F. Farouz, S. Thies, and F. Parhami, "Novel Oxysterols Have Pro-Osteogenic and Anti-Adipogenic Effects In Vitro and Induce Spinal Fusion In Vivo" J. Cellular Biochem. 2011, 112, 1673-1684. [pdf]

282. M. E. Jung and D. Yoo, "First Total Synthesis of Rhodexin A," Org. Lett. 2011, 13, 2698-2701. [pdf]

283. H. Wang, K. N. Houk, D. A. Allen, and M. E. Jung, "Computational Elucidation of the Origins of Reactivity and Selectivity in Non-Aldol Aldol Rearrangements of Cyclic Epoxides," Org. Lett. 2011, 13, 3238-3241. [pdf]

284. K. Kim, R. Damoiseaux, A. J. Norris, L. Rivina, K. Bradley, M. E. Jung, R. A. Gatti, R. H. Schiestl, W. H. McBride, "High Throughput Screening of Small Molecule Libraries for Modifiers of Radiation Responses," Int. J. Radiat. Biol. 2011, 87, 839-845. [pdf]

285. M. E. Jung and P. Koch, "An Efficient Synthesis of the Protected Carbohydrate Moiety of Brasilicardin A," Org. Lett. 2011, 13, 3710-3713. [pdf]

286. M. E. Jung and H. V. Chu, "Synthesis of BCD Tricylic Analogues of the Novel Cardiac Glycoside Rhodexin A," Tetrahedron Lett. 2011, 52, 4312-4314. [pdf]

287. M. E. Jung, J.-M. Ku, L. Du, H. Hu, and R. A. Gatti, "Synthesis and Evaluation of Compounds that Induce Readthrough of Premature Termination Codons," Bioorg. Med. Chem. Lett. 2011, 21, 5842-5848. [pdf]

288. M. E. Jung and P. Koch, "Mild and Selective Deprotection of PMB Ethers with Triflic Acid in Dichloromethane," Tetrahedron Lett. 2011, 52, 6051-6054. [pdf]

289. M. E. Jung and D. Yoo, "Stereoselective Synthesis of a Fully Protected C13-C23 Fragment of Tedanolide," Tetrahedron 2011, 67, 10281-10286. [pdf]

290. C. F. Regan, F. Pierre, M. K. Schwaebe, M. Haddach, M. E. Jung, and D. M. Ryckman, "A Facile Synthesis of 5-Halopyrimidine-4-carboxylic Acid Esters via a Minisci Reaction," Synlett 2012, 443-447. [pdf]

291. M. E. Jung, W.-J. Kim, N. K. Avliyakulov, M. Oztug, and M. J. Haykinson, "Synthesis and Validation of Cyanine-Based Dyes for DIGE," Ch. 6, "Differential Gel Electrophoresis (DIGE)," Springer-Verlag, 2012, pp. 67-88. [pdf]

292. N. J. Clegg, J. Wongvipat, C. Tran, S. Ouk, A. Dilhas, Y. Chen,K. Grillot, E. Bischoff, L. Cai, A. Aparicio, J. Kaufman, V. Arora, G. Shao, J. Qian, H. Zhao, G. Yang, J. Sensintaffar, T. Wasielewska, H. I. Scher, P. Smith-Jones, C. Bonnefous, J. Joseph, D. Darimont, M. Klang, E. De Stanchina, N. Wu, N. D. Smith, O. Ouerfelli, P. Rix, R. A. Heyman, M. E. Jung, C. Sawyers, and J. H. Hager, "Discovery and development of ARN-509, a novel Anti-androgen for the Treatment of Prostate Cancer," Cancer Research 2012, 72, 1494-1503. [pdf]

293. M. E. Jung and S. W. Yi, "Efficient Synthesis of threo β-Aminoalcohols from Amino-aldehydes via Chelation-controlled Additions. Total Synthesis of L-threo Sphingosine and Safingol,” Tetrahedron Lett. 2012, 53, 4216-4220. [pdf]

294. F. Stappenbeck, W. Xiao, M. Epperson, M. Riley, A. Priest, D. Huang, K. Nguyen, M. E. Jung, R. S. Thies and F. Farouz, "Novel Oxysterols Activate the Hedgehog Pathway and Induce Osteogenesis," Bioorg. Med. Chem. Lett. 2012, 22, 5893-5897. [pdf]

295. R. Kayali, J.-M. Ku, G. Khitrov, M. E. Jung, O. Prikhodko, and C. Bertoni, "Read-through compound 13 restores dystrophin expression and improves muscle function in the mdx mouse model for Duchenne muscular dystrophy," Hum. Mol. Genet. 2012, 21, 4007-4020. [pdf]

296. M. E. Jung and J. J. Chang, "Total Synthesis of the Proposed Structure of Mycosporulone: Structural Revision and an Unexpected Retro-Aldol–Aldol Reaction," Org. Lett. 2012, 14, 4898-4901. [pdf]

297. M. E. Jung and M. Guzaev, "Trimethylaluminum-Triflimide Complexes for the Catalysis of Highly Hindered Diels-Alder Reactions," Org. Lett. 2012, 14, 5169-5171. [pdf]

298. M. E. Jung and G. Deng, "Facile Synthesis of the 1-Monoester of 2-Ketoalkanedioic Acids, for example, α-Ketoglutarate," J. Org. Chem. 2012, 77, 11002-11005. [pdf]

299. M. E. Jung, F. Perez, C. F. Regan, S.-W. Yi, Q. Perron, "Phenylseleno Acrylate: New Ethylene Equivalent for Diels-Alder Reactions," Angew. Chem. 2013, 52, 2060-2062. Corrigendum: Angew. Chem. 2013, 52, 11963. [pdf]

300. K. J. Williams, J. P. Argus, Y. Zhu, M. Q. Wilks, B. N. Marbois, A. G. York, Y. Kidani, A. L. Pourzia, D. Akhavan, D. N. Lisiero, E. Komisopoulou, A. H. Henkin, H. Soto, B. T. Chamberlain, L. Vergnes, M. E. Jung, J. Z. Torres, L. M. Liau, H. R. Christofk, R. M. Prins, P. S. Mischel, K. Reue, T. G. Graeber, and S. J. Bensinger, "An essential requirement for the SCAP/SREBP signaling axis to protect cancer cells from lipotoxicity," Cancer Res. 2013, 73, 2850-2862. [pdf]

301. F. Vigant, J. Lee, A. Hollmann, L. Tanner, Z. Akyol-Ataman, G. Shui, H. Aguilar-Carreno, T. Yun, D. Zhang, D. Meriwether, G. Roman-Sosa, L. Robinson, T. Juelich, H. Buczkowski, S. Chou, M. A. R. B. Castanho, M. C. Wolf, A. Banyard, M. Kielian, S. Reddy, M. R. Wenk, M. Selke, N. C. Santos, A. Freiberg, M. E. Jung, and B. Lee, "A Mechanistic Paradigm for Broad-Spectrum Antivirals that Target Virus-cell Fusion," PLOS Pathog. 2013, 9, e1003297. [pdf]

302. M. E. Jung and M. Guzaev, "Studies Toward the Enantiospecific Total Synthesis of Rhodexin A," J. Org. Chem. 2013, 78, 7518-7526. [pdf]

303. J. M. Murphy, A. L. Armijo, C. H. Lee, D. O. Campbell, Z. Li, H.-I Liao, J. T. Lee, D. Nathanson, W. R. Austin, J. Nomme, R. Darvish, T. Smith, Y. Su, H. R. Herschman, A. Alexandrova, S. Sadeghi, M. E. Phelps, A. Lavie, M. E. Jung, J. Czernin, N. Satyamurthy, and C. G. Radu, "Development of new deoxycytidine kinase inhibitors and non-invasive in vivo evaluation using Positron Emission Tomography," J. Med. Chem. 2013, 56, 6696-6708. [pdf]

304. L. Du, M. E. Jung, R. Damoiseaux, G. Completo, F. Fike, J.-M. Ku, S. Nahas, C. Pao, H. Hu, and R. A. Gatti, "A new series of novel small molecular weight compounds induce readthrough of all three types of nonsense mutations in the ATM gene," Molec. Ther. 2013, 21, 1653-1660. [pdf]

305. A. H. Chan, J. Wereszczynski, B. R. Amer, S. W. Yi, M. E. Jung, R.T. Clubb, and J. A. McCammon, "Discovery of Staphylococcus aureus Sortase A Inhibitors Using Virtual Screening and the Relaxed Complex Scheme," Chem. Biol. Drug Des. 2013, 82, 418-428. [pdf]

306. W. Zhong, J. R. Springstead, R. Al-Mubarak, S. Lee, R. Li, B. Emert, J. A. Berliner, and M. E. Jung, "An Epoxyisoprostane is a Major Regulator of Endothelial Cell Function," J. Med. Chem. 2013, 56, 8521-8532. [pdf]

307. M. E. Jung, M. Trzoss, J. M. Tsay, and S. Weiss, "A Bis-Phosphine Modified Peptide Ligand for Stable and Luminescent Quantum Dots in Aqueous Media," Synthesis 2013, 2426-2430. [pdf]

308. X. Rong, C. J. Albert, C. Hong, M. A. Duerr, B. T. Chamberlain, E. J. Tarling, A. Ito, J. Gao, B. Wang, P. A. Edwards, M. E. Jung, D. A. Ford, and P. Tontonoz, "LXRs regulate ER stress and inflammation through dynamic modulation of membrane phospholipid composition," Cell Metab. 2013, 18, 685-697. [pdf]

309. E. J. Gillespie, C.-L. Ho, K. Balaji, Z. Li, D. Thomas, D. L. Clemens, G. Deng, Y. Wang, H. Elsaesser, B. Tamilselvam, B. France, B. T. Chamberlain, S. R. Blanke, G. Cheng, D. Brooks, M. E. Jung, M. Manchester, J. Zink, J. Colicelli, R. Damoiseaux, and K. A. Bradley, "Selective Inhibitor of Endosomal Trafficking Pathways Exploited by Multiple Toxins and Viruses," Proc. Natl. Acad. Sci. U.S.A., 2013, P110, E4904-E4912, SE4904/1-SE4904/4. [pdf]

310. D. M. Janzen, D. Y. Paik, M. A. Rosales, B. Yep, D. Cheng, O. N. Witte, H. Kayadibi, C. M. Ryan, M. E. Jung, K. Faull, and S. Memarzadeh, "Tumor sensitivity to poly(ADP-ribose) polymerase (PARP) inhibition in vivo is regulated by circulating levels of estrogen," Mol. Cancer Ther. 2013, 12, 2917-2928. [pdf]

311. K.-D. Kim, S. Srikanth, Y.-V. Tan, M.-K. Yee, M. Jew, R. Damoiseaux, M. E. Jung, S. Shimizu, D. S. An, B. Ribalet, J. A. Waschek, and Y. Gwack, "Calcium Signaling via Orai1 is Essential for Induction of Nuclear Orphan Receptor Pathway to drive Th17 Differentiation," J. Immunol. 2014, 192, 110-122. [pdf]

312. F. Vigant, A. Hollmann, J. Lee, N. Santos, M. E. Jung, and B. Lee, "The Rigid Amphipathic Fusion Inhibitor dUY11 Acts through Photosensitization of Viruses," J. Virol. 2014, 88, 1849. [pdf]

313. X. Yan, S. Lee, B. G. Gugiu, L. Koroniak, Michael E. Jung, J. Berliner, J. Cheng, and R. Li, "Fatty Acid Epoxyisoprostane E2 Stimulates an Oxidative Stress Response in Endothelial Cells," Biochem. Biophys. Res. Commun. 2014, 444, 69-74. [pdf]

314. D. A. Nathanson, A. L. Armijo, M. Tom, Z. Li, E. Dimitrova, W. R. Austin, J. Nomme, D. O. Campbell, L. Ta, T. M. Le, J. T. Lee, R. Darvish, A. Gordin, L. Wei, H.-I. Liao, M. Wilks, C. Martin, S. Sadeghi, J. M. Murphy, N. Boulos, M. E., Phelps, K. F. Faull, H. R. Herschman, M. E. Jung, J. Czernin, A. Lavie, and C. G. Radu, "Co-targeting of convergent nucleotide biosynthetic pathways for leukemia eradication," J. Exper. Med. 2014, 211, 473-486. [pdf]

315. M. E. Jung, B. T. Chamberlain, C.-L. Ho, E. J. Gillespie, and K. A. Bradley, "Photoaffinity Probes Developed from Structure-Activity Relationship Study Function as Irreversible Inhibitors of Anthrax Lethal Toxin," ACS Med. Chem. Letts. 2014, 5, 363-367. [pdf]

316. N. M. Evdokimov, G. Flores, P. M. Clark, M. E. Phelps, O. N. Witte, and M. E. Jung, "5-(2-[18F]Fluoroethyl)-4-methylthiazole Probe for Positron Emission Tomography of the Central Nervous System," Chem. Heterocycl. Compd. 2014, 330-334. [pdf]

317. A. W. Jacobitz, J. Wereszczynski, S. W. Yi, B. R. Amer, G. L. Huang, A. V. Nguyen, M. R. Sawaya, M. E. Jung, J. A. McCammon, and R.T. Clubb, "Structural and computational studies of the Staphylococcus aureus Sortase B-substrate complex reveal a substrate-stabilized oxyanion hole," J. Biol. Chem. 2014, 289, 8891-8902. [pdf]

318. M. E. Jung and G. Deng, "Synthesis of α-Diketones from Alkyl Aryl and Diarylalkynes using Mercuric Salts" Org. Lett. 2014, 16, 2142-2145. [pdf]

319. M. E. Jung, G. S. Lee, H. V. Pham, and K. N. Houk, "Palladium Hydride Promoted Stereoselective Isomerization of Unactivated Di-(Exo)methylenes to Endocyclic Dienes," Org. Lett. 2014, 16, 2382-2385. [pdf]

320. T. Sallam, A. Ito, X. Rong, J. Kim, C. van Stijn, B. T. Chamberlain, M. E. Jung, L. C. Chao, M. Jones, T. Gilliland, X. H. Wu, G. L. Su, R. K. Tangirala, P. Tontonoz, and C. Hong, "The macrophage LBP gene is an LXR target that promotes macrophage survival and atherosclerosis," J. Lipid Res., 2014, 55, 1120-1130. [pdf]

321. R. Chin, M. Pai, X. Fu, S. Diep, G. Jung, B. Lomenick, G. Deng, S. A. Whelan, G. C., Monsalve, H. R. Chang, C. F. Clarke, A. R. Frand, M. E. Jung, and J. Huang, "Alpha-ketoglutarate extends lifespan in Caenorhabditis elegans by a novel mechanism mediated by the ATP synthase and TOR," Nature, 2014, 510 (7505), 397-401. [pdf]

322. P. M. Clark, G. Flores, N. M. Evdokimov, M. N. McCracken, T. Chai, E. Nair-Gill, F. O’Mahony, S. W. Beaven, K. F. Faull, M. E. Phelps, M. E. Jung, and O. N. Witte, "Positron emission tomography probe demonstrates a striking concentration of ribose salvage in the liver," Proc. Natl. Acad. Sci. U.S.A. 2014, 111, E2866-E2874. [pdf]

323. M. E. Jung, T. A. Dwight, F. Vigant, M. E. Østergaard, E. S. Swayze, and P. P. Seth, "Synthesis and Duplex Stabilizing Properties of Fluorinated N-Methanocarbathymidine Analogs," Angew. Chem. 2014, 53, 9893-9897. [pdf]

324. S. R. Montgomery, T. Nargizyan, V. Meliton, S. Nachtergaele, R. Rohatgi, F. Stappenbeck, M. E. Jung, J. S. Johnson, B. Aghdasi, H. Tian, G. Weintraub, H. Inoue, E. Atti, S. Tetradis, R. C. Pereira, A. Hokugo, R. Alobaidaan, Y. Tan, T. J. Hahn, J. C. Wang, F. Parhami, "A Novel Osteogenic Oxysterol Compound for Therapeutic Development to Promote Bone Growth: Activation of Hedgehog Signaling and Osteogenesis through Smoothened Binding," J. Bone Miner. Res. 2014, 29, 1872-1885. [pdf]

325. M. E. Østergaard, T. A. Dwight, A. Berdeja, E. S. Swayze, M. E. Jung, and P. P. Seth, "A Comparison of Duplex Stabilizing "Properties of 2’-Fluorinated Nucleic Acid Analogs with Furanose and Non-Furanose Sugar Rings," J. Org. Chem. 2014, 79, 8877-8881. [pdf]

326. M. E. Jung and G. S. Lee, "Efficient Synthesis of Highly Substituted Adamantanones from Bicyclo[3.3.1]nonanes," J. Org. Chem. 2014, 79, 10547-10552. [pdf]

327. J. Nomme, Z. Li, R. M. Gipson, J. Wang, A. L. Armijo, T. Le, S. Poddar, T. Smith, B. D. Santarsiero, H.-A. Nguyen, J. Czernin, A. N. Alexandrova, M. E. Jung, C. G. Radu, and A. Lavie, "Structure-guided development of deoxycytidine kinase inhibitors with nanomolar affinity and improved metabolic stability," J. Med. Chem. 2014, 57, 9480-9494. [pdf]

328. C. Hong, S. M. Marshall, A. L. McDaniel, M. Graham, J. D. Layne, L. Cai, E. Scotti, R. Boyadjian, J. Kim, B. T. Chamberlain, R. K. Tangirala, M. E. Jung, L. Fong, R. Lee, S. G. Young, R. E. Temel, and P. Tontonoz, "The LXR-Idol Axis Differentially Regulates Plasma LDL Levels in Primates and Mice," Cell Metab. 2014, 20, 910-918. [pdf]

329. M. Manoharan, K. N. Jayaprakash, J. Willoughby, A. Chan, K. Charisse, R. Alam, Q. Wang, M. Hoekstra, P. Kandasamy, A. Kelin, S. Milstein, N. Taneja, J. O’Shea, S. Shaikh, L. Zhang, R. van der Sluis, T. van Berkel, M. E. Jung, A. Akinc, R. Hutabarat, S. Kuchimanchi, Satya; K. Fitzgerald, T. Zimmermann, M. Maier, R. Kallanthottathil, "Multivalent N-Acetylgalactosamine-Conjugated siRNA Localizes in Hepatocytes and Elicits Robust RNAi-mediated Gene Silencing," J. Am. Chem. Soc. 2014, 136, 16958-16961. [pdf]

330. J. Escamilla, C. Liu, S. Priceman, J. Sung, F. Pouliot, C. Magyar, Z. Jiang, J. Xu, G. Deng, B. West, G. Bollag, Y. Fradet, L. Lacombe, M. E. Jung, J. Huang, and L. Wu, "CSF1 Receptor Targeting In Prostate Cancer Reverses Macrophage-Mediated Resistance to Androgen Blockade Therapy," Cancer Res., 2015, 75, 950-962. [pdf]

331. M. E. Jung and D. L. Sun, "Trapping of Payne Rearrangement Intermediates with Arylselenide Anions," Tetrahedron Lett. 2015, 56, 3082-3085. [pdf]

332. N. M. Evdokimov, P. M. Clark, G. Flores, T. Chai, K. F. Faull, M. E. Phelps, O. N. Witte and M. E. Jung, "[18F]-2-Deoxy-2-fluororibose is a sensitive PET probe for studying liver function in vivo," J. Med. Chem. 2015, 58, 5538-5547. [pdf]

333. M. E. Jung, B. T. Chamberlain, P. Koch, and K. V. Niazi, "Synthesis and Bioactivity of a Brasilicardin A Analogue Featuring a Simplified Core," Org. Lett. 2015, 17, 3608-3611. [pdf]

334. X. Fu, R. M. Chin, L. Vergnes, H. Hwang, G. Deng, Y. Xing, M. Y. Pai, S. Li, L. Ta, F. Fazlollahi, C. Chen, R. M. Prins, M. A. Teitell, D. A. Nathanson, A. Lai, K. F. Faull, M. Jiang, S. G. Clarke, T. F. Cloughesy, T. G. Graeber, D. Braas, H. R. Christofk, M. E. Jung, K. Reue, and J. Huang, "2-Hydroxyglutarate Inhibits ATP Synthase and mTOR Signaling," Cell Metab. 2015, 22, 508-515. [pdf]

335. Chan, A. H.; Yi, S. W.; Terwilliger, A. L.; Maresso, A. W.; Jung, M. E. and Clubb, R. T., "Structure of the Bacillus anthracis sortase A enzyme bound to its sorting signal: a flexible amino-terminal appendage modulates substrate access," J. Biol. Chem. 2015, 290, 25461-25474. [pdf]

336. M. E. Jung, C. A. Roberts, F. Perez, H. V. Pham, L. Zou, K. N. Houk, "Thermodynamic Control of Isomerizations of Bicyclic Radicals: The Interplay of Ring Strain and Radical Stabilization," Org. Lett. 2016, 18, 32-35. [pdf]

337. J. Y. Chen, C. Tran, L. Hwang, G. Deng, M. E. Jung, K. F. Faull, M. S. Levine, and C. Cepeda, "Partial Amelioration of Peripheral and Central Symptoms of Huntington’s Disease via Modulation of Lipid Metabolism," J. Huntingtons Dis. 2016, 5, 65-81. [pdf]

338. B. Holmes, J. Lee, K. A. Landon, A. Benavides-Serrato, T. Bashir, M. E. Jung, A. Lichtenstein, and J. Gera, "Mechanistic Target of Rapamycin (mTOR) Inhibition Synergizes with Reduced IRES-mediated Translation of Cyclin D1 and c-MYC to Treat Glioblastoma," J. Biol. Chem. 2016, 291, 14146-14159. [pdf]

339. A. W. Jacobitz, E. B. Naziga, S. W. Yi, S. A. McConnell, R. Peterson, M. E. Jung, R. T. Clubb, and J. Wereszczynski, "The “lid” in the Streptococcus pneumoniae SrtC1 sortase adopts a rigid structure that regulates substrate access to the active site," J. Phys. Chem. B 2016, 120, 8302-8312. [pdf]

340. M. E. Jung, D. L. Sun, T. A. Dwight, P. Yu, W. Li, and K. N. Houk, "Synthesis of 2-Ethenylcyclopropyl Aryl Ketones via Intramolecular SN2-like Displacement of an Ester," Org. Lett. 2016, 18, 5138-5141. [pdf]

341. Y. Shi, T. R. Daniels-Wells, P. Frost, J. Lee, R. S. Finn, C. Bardeleben, M. L. Penichet, M. E. Jung, J. Gera, and A. Lichtenstein, "An Inhibitor of DEPTOR-mTOR Binding Induces Significant Cytotoxicity against Multiple Myeloma Cells," Cancer Res. 2016, 76, 5822-5831. [pdf]

342. B. F. Balmer, R. L. Powers, T. Zhang, J. Lee, F. Vigant, B. Lee, M. E. Jung, M. K. Purcell, K. Snekvik and H. C. Aguilar, "Inhibition of an aquatic rhabdovirus demonstrates promise of a broad-spectrum antiviral for use in aquaculture," J. Virol. 2017, 91, e02181-16/1-e02181-16/12. [pdf]

343. A. Benavides-Serrato, J. Lee, B. Holmes, K. A. Landon, T. Bashir, M. E. Jung, A. Lichtenstein, and J. Gera, "Specific blockade of Rictor-mTOR association inhibits mTORC2 activity and is cytotoxic in glioblastoma," PLOS One 2017, 12, e0176599. [pdf]

344. M. E. Østergaard, J. Nichols, T. A. Dwight, W. Lima, M. E. Jung, E. S. Swayze, and P. P. Seth, "Fluorinated Nucleoside Modifications Modulate Allel Selectivity of SNP Targeting Antisense Oligonucleotides," Mol. Ther.--Nucleic Acids 2017, 7, 20-30.[pdf]

345. A. H. Chan, S. W. Yi, E. M. Weiner, B. R. Amer, C. Sue, J. Wereszczynski, C. Dillen, S. Senese, J. Z. Torres, J. A. McCammon, L. S. Miller, M. E. Jung, and R. T. Clubb, "NMR Structure-Based Optimization of Staphylococcus aureus Sortase A Pyridazinone Inhibitors," Chem. Biol. Drug Des. in press. [pdf]


NOTE: Check out the interesting (and unusual) publication by M. E. Jung: Crostic No. 49 in Crostics, No. 115, Simon & Schuster, New York, NY, ed. T. H. Middleton, 1996. [pdf]
 

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