Pd(II)-catalyzed enantioselective C-H olefination of diphenylacetic acids.

ABSTRACT: Pd(II)-catalyzed enantioselective C-H olefination of diphenylacetic acid substrates has been achieved through the use of monoprotected chiral amino acid ligands. The absolute configuration of the resulting olefinated products is consistent with that of a proposed C-H insertion intermediate.

SUBMITTER: Shi BF 

PROVIDER: S-EPMC2806936 | biostudies-literature | 2010 Jan

REPOSITORIES: biostudies-literature