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Issue 15, 1997
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Diastereoselective intramolecular photochemical [2 + 2]cycloaddition reactions of tethered l-(+)-valinol derivedtetrahydrophthalimides

Abstract

Intramolecular photochemical [2 + 2] cycloaddition of allyl alcohol linked to amino acid derived 3,4,5,6-tetrahydrophthalimides, either via a carbonate or silicon tether, gives the corresponding cyclobutanes in excellent yield with diastereoselectivities as high as 8:1.

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Article type: Paper
DOI: 10.1039/A702386C
Citation: Chem. Commun., 1997,0, 1385-1386
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    Diastereoselective intramolecular photochemical [2 + 2] cycloaddition reactions of tethered l-(+)-valinol derived tetrahydrophthalimides

    K. I. Booker-Milburn, S. Gulten and A. Sharpe, Chem. Commun., 1997, 0, 1385
    DOI: 10.1039/A702386C

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