Metal-mediated oxidation reactions play an important role in biological processes and in abiological reactions used in organic synthesis. The function of a large proportion of these reactions is the transfer of groups containing heteroatoms such as nitrogen, oxygen, phosphorus and sulfur to organic molecules. Many of these processes have been postulated to proceed via metal complexes that contain reactive metal-heteroatom multiple bonds. However, exploration of the chemistry of these functionalities, extending and applying their reactions to transformations useful in organic synthesis, and understanding the mechanisms of their reactions, lag substantially behind what is known about analogous processes involving metal-carbon multiple bonds (carbene complexes). As a result, there is a need for development of new chemistry based on isolable complexes that bear metal-heteroatom multiple bonds. ? ? The overall goal of this proposal is the development of systematic methods for the synthesis of complexes containing metal-heteroatom multiple bonds, the development of new stoichiometric and catalytic reactions in which these bonds play a central role that can be applicable to organic synthesis, and the study of the scope and mechanisms of these reactions. A significant part of the project will be devoted to the synthesis of chiral, enantioresolved complexes that can be used in the development of stereoselective transformations leading to enantioenriched organic compounds with new bonds between carbon and heteroatoms. Specific targets for the proposed grant period will be the development of (1) stereoselective, catalytic and stoichiometric carboamination of alkynes; (2) catalytic diimination of unsaturated substrates; (3) highly regio- and stereoselective allylic substitutions of allyl halides and ethers; (4) methods for desymmetrization of meso-epoxides; (5) reactive and enantioselective catalysts for the hydroamination of alkenes; (6) catalytic hydrophosphination of alkenes and alkynes; (7) exploration of the addition of organic C-H bonds to metal-heteroatom multiple bonds. ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
2R01GM025459-28A1
Application #
7030618
Study Section
Synthetic and Biological Chemistry A Study Section (SBCA)
Program Officer
Schwab, John M
Project Start
1978-08-01
Project End
2009-12-31
Budget Start
2006-01-03
Budget End
2006-12-31
Support Year
28
Fiscal Year
2006
Total Cost
$318,586
Indirect Cost
Name
University of California Berkeley
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
124726725
City
Berkeley
State
CA
Country
United States
Zip Code
94704
Tomson, Neil C; Arnold, John; Bergman, Robert G (2010) Halo, Alkyl, Aryl, and Bis(imido) Complexes of Niobium Supported by the beta-Diketiminato Ligand. Organometallics 29:2926-2942
Tomson, Neil C; Arnold, John; Bergman, Robert G (2010) Synthesis, Characterization, and Reactions of Isolable (?-Diketiminato)Nb(III) Imido Complexes. Organometallics 29:5010-5025
Schomaker, Jennifer M; Toste, F Dean; Bergman, Robert G (2009) Cobalt-mediated [3 + 2]-annulation reaction of alkenes with alpha,beta-unsaturated ketones and imines. Org Lett 11:3698-700
Tomson, Neil C; Yan, Andrew; Arnold, John et al. (2008) An unusally diverse array of products formed upon carbonylation of a dialkylniobium complex. J Am Chem Soc 130:11262-3
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Krinsky, Jamin L; Anderson, Laura L; Arnold, John et al. (2008) Oxygen-centered hexatantalum tetradecaimido cluster complexes. Inorg Chem 47:1053-66
Krinsky, Jamin L; Anderson, Laura L; Arnold, John et al. (2007) Synthesis and properties of oxygen-centered tetradecaimido hexatantalum clusters. Angew Chem Int Ed Engl 46:369-72
Fox, Richard J; Lalic, Gojko; Bergman, Robert G (2007) Regio- and stereospecific formation of protected allylic alcohols via zirconium-mediated S(N)2'substitution of allylic chlorides. J Am Chem Soc 129:14144-5
Hoyt, Helen M; Bergman, Robert G (2007) Kinetic control and multiple mechanisms for C-H bond activation by a Zr=N complex. Angew Chem Int Ed Engl 46:5580-2

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