The ability to control the alkylation of organic substrates becomes ever more powerful by using metal catalysts. Among the major benefits of metal catalysis is the possibility to perform such processes asymmetrically using only catalytic amounts of the chiral inducing agent which is a ligand to the metal of the catalyst. A unique aspect of asymmetric metal-catalyzed processes is the fact that many mechanisms exist for stereoinduction. Furthermore, with the use of the same catalyst system, many types of bonds including but not limited to C-C, C-N, C-O, C-S, C-P, and C-H can be formed asymmetrically. An overview of this process using palladium- and molybdenum-based metals being developed in my laboratories and how it influences strategy in synthesizing bioactive molecular targets is presented.
机构:
Department of Chemistry, Stanford University, Stanford, CA 94305-5080, United StatesDepartment of Chemistry, Stanford University, Stanford, CA 94305-5080, United States
Trost, Barry M.
Shen, Hong C.
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Department of Chemistry, Stanford University, Stanford, CA 94305-5080, United StatesDepartment of Chemistry, Stanford University, Stanford, CA 94305-5080, United States
Shen, Hong C.
Dong, Li
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Department of Chemistry, Stanford University, Stanford, CA 94305-5080, United StatesDepartment of Chemistry, Stanford University, Stanford, CA 94305-5080, United States
Dong, Li
Surivet, Jean-Philippe
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Department of Chemistry, Stanford University, Stanford, CA 94305-5080, United StatesDepartment of Chemistry, Stanford University, Stanford, CA 94305-5080, United States
Surivet, Jean-Philippe
Sylvain, Catherine
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Department of Chemistry, Stanford University, Stanford, CA 94305-5080, United StatesDepartment of Chemistry, Stanford University, Stanford, CA 94305-5080, United States
Sylvain, Catherine
Journal of the American Chemical Society,
2004,
126
(38):
: 11966
-
11983