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Issue 29, 2013
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Conformationally restricted pyrrolidines by intramolecular [2+2] photocycloaddition reactions

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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

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Publication details

The article was received on 29 Jan 2013, accepted on 25 Feb 2013 and first published on 06 Mar 2013


Article type: Communication
DOI: 10.1039/C3CC40757H
Citation: Chem. Commun., 2013,49, 2989-2991
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    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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