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Evidence for the importance of conformational equilibria in Rh-diphosphine complexes for the enantioselection in Rh-catalyzed asymmetric hydrogenation
Authors:Hideyuki Tsuruta  Kentaro Yamaguchi
Affiliation:a Department of Chemistry, Faculty of Science, Chiba University, Yayoi-cho, Inage-ku, Chiba 263-8522, Japan
b Chemical Analysis Center, Chiba University, Yayoi-cho, Inage-ku, Chiba 263-8522, Japan
c COE Laboratory, Department of Chemistry, Graduate School of Science, Tohoku University, Aoba-ku, Sendai 980-8578, Japan
Abstract:The conformations of the chelate cycles in the X-ray structures of norbornadiene- and cyclooctadiene-rhodium complexes of (R,R)-1,2-bis[(o-methylphenyl)phenylphosphino]ethane are dramatically different. Nevertheless, they demonstrate the same sense of enantioselection in asymmetric hydrogenation of dehydroamino acids.
Keywords:Asymmetric hydrogenation   Chiral diphosphines   Chiral rhodium complexes   Sense of enantioselection
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