Issue 6, 1995
From the journal:

Journal of the Chemical Society, Chemical Communications

Enantioselective intramolecular [2 + 2] photocycloaddition reaction of N-allyl-3-oxo-1-cyclohexenecarboxamides in inclusion crystals with chiral host compounds

Fumio Toda,   Hisakazu Miyamoto  and  Siro Kikuchi  

Abstract

Photoirradiation of powdered inclusion crystals of the title compounds with chiral host compounds derived from tartaric acid in a water suspension give the optically active [2 + 2] photocyclisation products.

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Article information

DOI
https://doi.org/10.1039/C39950000621
Article type
Paper

J. Chem. Soc., Chem. Commun., 1995, 621-622

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Enantioselective intramolecular [2 + 2] photocycloaddition reaction of N-allyl-3-oxo-1-cyclohexenecarboxamides in inclusion crystals with chiral host compounds

F. Toda, H. Miyamoto and S. Kikuchi, J. Chem. Soc., Chem. Commun., 1995, 621 DOI: 10.1039/C39950000621

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