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The Catalytic Asymmetric α‐Benzylation of Aldehydes
Authors:Prof. Dr. Benjamin List  Dr. Ilija Čorić  Dr. Oleksandr O. Grygorenko  Philip S. J. Kaib  Prof. Dr. Igor Komarov  Dr. Anna Lee  Markus Leutzsch  Dr. Subhas Chandra Pan  Andrey V. Tymtsunik  Manuel van Gemmeren
Affiliation:1. Max‐Planck‐Institut für Kohlenforschung, Kaiser Wilhelm‐Platz 1, 45470 Mülheim an der Ruhr (Germany);2. Taras Shevchenko National University of Kyiv, Volodymyrska Street 60, Kyiv (Ukraine)
Abstract:The first aminocatalyzed α‐alkylation of α‐branched aldehydes with benzyl bromides as alkylating agents has been developed. Using a sterically demanding proline derived catalyst, racemic α‐branched aldehydes are reacted with alkylating agents in a DYKAT process to give the corresponding α‐alkylated aldehydes with quaternary stereogenic centers in good yields and high enantioselectivities.
Keywords:α  ‐alkylation  α  ‐branched aldehydes  DYKATt  enamine catalysis  organocatalysis
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