Issue 8, 2015

Asymmetric Michael addition of α-fluoro-α-nitro esters to nitroolefins: towards synthesis of α-fluoro-α-substituted amino acids

Abstract

α-Fluoro-α-nitro esters were used as reaction partners in Michael addition to nitroalkenes, and the products were obtained in excellent chemical yields and with high enantioselectivities. Moreover, α-fluoro-α-amino ester with a quaternary α-carbon was prepared for the first time.

Graphical abstract: Asymmetric Michael addition of α-fluoro-α-nitro esters to nitroolefins: towards synthesis of α-fluoro-α-substituted amino acids

Supplementary files

Article information

Article type
Paper
Submitted
26 Nov 2014
Accepted
10 Dec 2014
First published
07 Jan 2015

Org. Biomol. Chem., 2015,13, 2350-2359

Asymmetric Michael addition of α-fluoro-α-nitro esters to nitroolefins: towards synthesis of α-fluoro-α-substituted amino acids

J. Kwiatkowski and Y. Lu, Org. Biomol. Chem., 2015, 13, 2350 DOI: 10.1039/C4OB02486A

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