Issue 37, 2017

Enantioselective electrophilic cyanation of β-keto amides catalysed by a cinchona organocatalyst

Abstract

An operationally simple protocol for the enantioselective electrophilic α-cyanation of β-keto amides catalyzed by cinchona-derived catalysts has been demonstrated. The resulting products could be obtained with good to high enantioselectivities (up to 88% ee) and with excellent yields (up to 94%) by employing the mild active 4-acetylphenyl cyanate as the cationic cyano source in the catalytic asymmetric α-cyanation reaction.

Graphical abstract: Enantioselective electrophilic cyanation of β-keto amides catalysed by a cinchona organocatalyst

Supplementary files

Article information

Article type
Communication
Submitted
19 Jul 2017
Accepted
01 Sep 2017
First published
01 Sep 2017

Org. Biomol. Chem., 2017,15, 7753-7757

Enantioselective electrophilic cyanation of β-keto amides catalysed by a cinchona organocatalyst

P. G. Karmaker, J. Qiu, D. Wu, M. Reng, Z. Yang, H. Yin and F. Chen, Org. Biomol. Chem., 2017, 15, 7753 DOI: 10.1039/C7OB01782K

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