Issue 34, 2011

Visible light mediated azomethine ylide formation—photoredox catalyzed [3+2] cycloadditions

Abstract

The synthesis of highly functionalised N-heterocycles has been achieved by the visible light mediated photoredox conversion of tertiary amines to azomethine ylides and their further reaction with maleimide derivatives as dipolarophiles.

Graphical abstract: Visible light mediated azomethine ylide formation—photoredox catalyzed [3+2] cycloadditions

Supplementary files

Article information

Article type
Communication
Submitted
20 Jun 2011
Accepted
08 Jul 2011
First published
27 Jul 2011

Chem. Commun., 2011,47, 9615-9617

Visible light mediated azomethine ylide formation—photoredox catalyzed [3+2] cycloadditions

M. Rueping, D. Leonori and T. Poisson, Chem. Commun., 2011, 47, 9615 DOI: 10.1039/C1CC13660G

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