Issue 4, 2015

Enantioselective synthesis of benzoindolizidine derivatives using chiral phase-transfer catalytic intramolecular domino aza-Michael addition/alkylation

Abstract

An efficient and enantioselective strategy to synthesize benzoindolizidines from α,β-unsaturated amino ketones via domino intramolecular aza-Michael addition/alkylation was developed. These reactions were enabled by cinchona alkaloid-derived quaternary ammonium salts as the phase-transfer catalyst. A variety of benzoindolizidines were prepared in good yields (up to 93%) and enantioselectivities (up to 92.8 : 7.2 er).

Graphical abstract: Enantioselective synthesis of benzoindolizidine derivatives using chiral phase-transfer catalytic intramolecular domino aza-Michael addition/alkylation

Supplementary files

Article information

Article type
Paper
Submitted
20 Oct 2014
Accepted
13 Nov 2014
First published
14 Nov 2014

Org. Biomol. Chem., 2015,13, 1179-1186

Enantioselective synthesis of benzoindolizidine derivatives using chiral phase-transfer catalytic intramolecular domino aza-Michael addition/alkylation

J. Guo and S. Yu, Org. Biomol. Chem., 2015, 13, 1179 DOI: 10.1039/C4OB02227K

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