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                |  |  |   Craig A. MerlicB.S. 1982, University of California, Davis; Ph.D. 1988, University
                  of Wisconsin, Madison; NIH Postdoctoral Fellow 1988-1989, Princeton
                  University; National Science Foundation Young Investigator Award,
                  1992-1997; Camille Dreyfus Teacher-Scholar Award, 1994-1999;
                  Alfred P. Sloan Research Fellowship, 1995-1997.
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                |  RESEARCH
                  INTERESTSOur research program in organic and organometallic chemistry
                  encompasses synthetic organic, synthetic organometallic, and
                  physical organometallic chemistry. Research goals include discovery
                  of new reactions and catalysts, development of synthetic methods,
                  new techniques for asymmetric synthesis, determination of reaction
                  mechanisms, synthesis of bioactive natural products and development
                  of organometallic complexes for materials research. The development
                  of new chemistry using organometallic species is a rich and fertile
                  area due to the unique ability of transition metal fragments
                  to impart special reactivity, selectivity, and stability upon
                  bonded organic moieties. Our research draws on these features
                  to address problems in organic synthesis. Organometallic Radical
                  Reactions for Stereoselective SynthesisOrganometallic radical reactions are being investigated as
                  new methods for carbon-carbon bond formation. By using transition
                  metal fragments totemplate the reactions of organic moieties,
                  control of chemoselectivity, regiochemistry and stereochemistry
                  in radical cyclizations is feasible. A wide array of organometallic
                  compounds are employed including iron olefin complexes, cobalt
                  alkyne complexes, iron triene complexes, chromium carbene complexes
                  and arene chromium complexes. The later are used for asymmetric
                  synthesis where both enantiomers of a product are available from
                  a single starting enantiomer. Applications of the newly developed
                  methods to the syntheses of biologically active products such
                  as antitumor agents, unnatural sugars, and antibiotics are under
                  investigation.
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                | Synthesis Via Metal-Mediated
                  Pericyclic Reactions and Fischer Carbene ComplexesWe are exploring fundamentally new types
                  of pericyclic reactions by incorporating metal fragments into
                  reacting polyene arrays. The metals can participate directly
                  in pericyclic reactions or can serve as templates to control
                  reaction selectivity. Examples include a variety of annulations
                  employing chromium carbene complexes, while second generation
                  reactions will employ metal fragments catalytically. Topics we
                  seek to address in organometallic pericyclic reactions include
                  reaction mechanisms, selectivity rules, substrate variability
                  and synthetic applications. These new methods are being applied
                  in the synthesis of a number of structurally diverse antibiotic,
                  antiimflammatory and antitumor agents.
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                |  Asymmetric Synthesis
                  and CatalysisWhile stoichiometric implementation of transition metal organometallic
                  chemistry provides for unique molecular transformations, the
                  real power of transition metal complexes lies in catalysis. Single
                  catalytic reactions can replace multiple steps in traditional
                  organic synthesis and do so with lower costs in an environmentally
                  friendly manner. Catalysts are under investigation for precesses
                  including asymmetric synthesis, carbon-heteroatom bond formation,
                  multicomponent coupling, cycloisomerizations and pericyclic reactions.
                  Most of these focus on the use of homogeneous palladium and ruthenium
                  catalysis. New methods of catalyst immobilization that facilitate
                  recycling and reuse are also being explored.
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   REPRESENTATIVE PUBLICATIONS1. Merlic, C.A.; Xu, D. "Cyclization Reactions of Dienyl
            Chromium Carbene Complexes. Entry to Ortho Substituted Aromatic
            Alcohols via a Designed Photoreaction" J. Am. Chem. Soc.
            1991, 113, 7418-7420. 2. Merlic, C.A.; Xu, D. "Intermolecular Radical Reactions
            of Unsaturated Chromium and Tungsten Carbene Complexes,"
            J. Am. Chem. Soc. 1991, 113, 9855-9856. 3. Merlic, C. A.; Xu, D.; Khan, S. I. "Synthesis, Structure
            and Reactivity of Cyclic Arene Chromium Carbene Complexes"
            Organometallics 1992, 11, 412-418. 4. Merlic, C. A.; Burns, E. E.; Xu, D.; Chen, S. Y. "Aminobenzannulation
            Via Metathesis of Isonitriles Using Chromium Carbene Complexes"
            J. Am. Chem. Soc. 1992, 114, 8722-8724. 5. Merlic, C. A.; Xu, D; Gladstone, B. "Aminobenzannulation
            Via Photocyclization Reactions of Chromium Dienyl(Amino)carbene
            Complexes. Synthesis of Ortho Amino Aromatic Alcohols" J.
            Org. Chem. 1993, 58, 538-545. 6. Merlic, C. A.; Bendorf, H. D. "Titanium-Templated
            [4+2] Oxidative Cycloadditions: A Facile Route to 7-Hydroxynorbornenes"
            Organometallics 1993, 12, 559-564. 7. Merlic, C. A.; Burns, E. E. "Chemoselectivity in the
            Isonitrile Metathesis Route to Aromatic Amines" Tetrahedron
            Lett. 1993, 34, 5401-5404. 8. Merlic, C. A.; Bendorf, H. D. "Cyclopropanation of
            C60 Via a Fischer Carbene Complex" Tetrahedron Lett.
            1994, 35, 9529-9532. 9. Merlic, C. A.; Albaneze, J. "Rapid Synthesis of Functionalized,
            Alkoxy-Substituted, Allylstannanes from Carbene Complexes"
            Tetrahedron Lett. 1995, 36, 1007-1010. 10. Merlic, C. A.; Albaneze, J. "Synthesis of Alkoxy-Substituted
            Allenyl- and Propargylstannane Reagents from Carbene Complexes"
            Tetrahedron Lett. 1995, 36, 1011-1014. 11. Merlic, C. A.; Motamed, S.; Quinn, B. "Structure
            Determination and Synthesis of Fluoro Nissl Green: An RNA Binding
            Fluorochrome" J. Org. Chem. 1995, 60,
            3365-3369. 12. Merlic, C. A.; Pauly, M. E. "Ruthenium-Catalyzed
            Cyclizations of Dienylalkynes Via Vinylidene Intermediates"
            J. Am. Chem. Soc. 1996, 118, 11319-11320. 13. Merlic, C. A.; McInnes, D. M.; You, Y. "Synthesis
            of Indolocarbazoles via Annulations of Chromium Carbene Complexes"
            Tetrahedron Lett. 1997, 38, 6787-6790. 14. Merlic, C. A.; McInnes, D. M. "Synthesis of Indolocarbazoles
            via Sequential Palladium Catalyzed Cross Coupling and Benzannulation
            Reactions" Tetrahedron Lett. 1997, 38,
            7661-7664. 15. Merlic, C. A.; Wu, F. "Synthesis of b-Keto Fischer
            Carbene Complexes" Journal of Organometallic Chemistry
            1998, 553, 183-191. 16. Merlic, C. A.; Walsh, J. C. "Completely Diastereoselective
            Radical Reactions Using Arenechromium Tricarbonyl Complexes"
            Tetrahedron Lett. 1998, 39, 2083-2086. 17. Merlic, C. A.; Walsh, J. C.; Tantillo, D. J.; Houk, K.
            N. "Chemical Hermaphroditism: The Potential of the Cr(CO)3
            Moiety to Stabilize Transition States and Intermediates with
            Anion Cationic, Radical Character at the Benzylic Position"
            J. Am. Chem. Soc. 1999, 121, 3596-3606. 18. Merlic, C. A.; Aldrich, C. C.; Albaneze-Walker, J.; Saghatelian,
            A. "Carbene Complexes in the Synthesis of Complex Natural
            Products: Total Synthesis of the Calphostins" J. Am.
            Chem. Soc., 2000, 122, 3224-3225. For a complete list of publications,
            go to Merlic Page 2.
 

 ADDITIONAL INFORMATIONThe
            Merlic Research Group Page
 
 
 
 
              
                | Email: merlic@chem.ucla.edu Phone: 310-825-5466
                  Fax: 310-206-3722
 |  | University of California, Los Angeles Department of Chemistry and Biochemistry
 607 Charles E. Young Drive East
 Los Angeles, CA 90095-1569
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   Updated on 6/22/00 by Alice Ramirez: alice@chem.ucla.edu
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