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Issue 60, 2015
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N-Heterocyclic carbene-catalyzed [3+3] cyclocondensation of bromoenals with aldimines: highly enantioselective synthesis of dihydropyridinones

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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

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Publication details

The article was received on 04 Jun 2015, accepted on 16 Jun 2015 and first published on 16 Jun 2015


Article type: Communication
DOI: 10.1039/C5CC04593B
Chem. Commun., 2015,51, 12040-12043

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    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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