Issue 15, 1997
From the journal:

Chemical Communications

Diastereoselective intramolecular photochemical [2 + 2] cycloaddition reactions of tethered l-(+)-valinol derived tetrahydrophthalimides

Kevin I. Booker-Milburn,   Sirin Gulten  and  Andrew Sharpe  

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 information

DOI
https://doi.org/10.1039/A702386C
Article type
Paper

Chem. Commun., 1997, 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, 1385 DOI: 10.1039/A702386C

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