Issue 29, 2013

Conformationally restricted pyrrolidines by intramolecular [2+2] photocycloaddition reactions

Abstract

Intramolecular [2+2] photocycloaddition reactions of diversely substituted N-Boc protected 4-(allylaminomethyl)-2(5H)-furanones resulted in rigid products (53–75%) with three spatially defined positions for further functionalisation.

Graphical abstract: Conformationally restricted pyrrolidines by intramolecular [2+2] photocycloaddition reactions

Supplementary files

Article information

Article type
Communication
Submitted
29 Jan 2013
Accepted
25 Feb 2013
First published
06 Mar 2013

Chem. Commun., 2013,49, 2989-2991

Conformationally restricted pyrrolidines by intramolecular [2+2] photocycloaddition reactions

D. A. Fort, T. J. Woltering, M. Nettekoven, H. Knust and T. Bach, Chem. Commun., 2013, 49, 2989 DOI: 10.1039/C3CC40757H

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