Issue 56, 2015

Construction of an all-carbon quaternary stereocenter by organocatalytic enantioselective α-functionalization of α-substituted β-ketocarbonyls with electron deficient vinylarenes

Abstract

A chiral amine catalyzed enantioselective α-functionalization of α-substituted β-ketocarbonyls with electron-deficient vinylarenes has been developed to construct the dicarbonyl products with the formation of a chiral all-carbon quaternary stereocenter. The products can be used for the efficient synthesis of useful but challenging chiral quaternary centered pyrazolones.

Graphical abstract: Construction of an all-carbon quaternary stereocenter by organocatalytic enantioselective α-functionalization of α-substituted β-ketocarbonyls with electron deficient vinylarenes

Supplementary files

Article information

Article type
Communication
Submitted
29 Apr 2015
Accepted
01 Jun 2015
First published
01 Jun 2015

Chem. Commun., 2015,51, 11221-11224

Author version available

Construction of an all-carbon quaternary stereocenter by organocatalytic enantioselective α-functionalization of α-substituted β-ketocarbonyls with electron deficient vinylarenes

S. Liu, M. Tong, Y. Yu, H. Xie, H. Li and W. Wang, Chem. Commun., 2015, 51, 11221 DOI: 10.1039/C5CC03562G

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