Issue 60, 2015

N-Heterocyclic carbene-catalyzed [3+3] cyclocondensation of bromoenals with aldimines: highly enantioselective synthesis of dihydropyridinones

Abstract

The N-heterocyclic carbene-catalyzed [3+3] cyclocondensation of bromoenals and aldimines was developed to give the corresponding dihydropyridinones in good yields with excellent enantioselectivities.

Graphical abstract: N-Heterocyclic carbene-catalyzed [3+3] cyclocondensation of bromoenals with aldimines: highly enantioselective synthesis of dihydropyridinones

Supplementary files

Article information

Article type
Communication
Submitted
04 Jun 2015
Accepted
16 Jun 2015
First published
16 Jun 2015

Chem. Commun., 2015,51, 12040-12043

N-Heterocyclic carbene-catalyzed [3+3] cyclocondensation of bromoenals with aldimines: highly enantioselective synthesis of dihydropyridinones

Z. Gao, X. Chen, H. Zhang and S. Ye, Chem. Commun., 2015, 51, 12040 DOI: 10.1039/C5CC04593B

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