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Issue 15, 1992
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Control of the stereochemistry in the photocyclisation of acrylanilides to 3,4-dihydroquinolin-2(1H)-ones. Delicate dependence on the host compound

Koichi Tanaka,  Osamu Kakinoki  and  Fumio Toda 

Abstract

The stereochemistry of the photocyclisation of acrylanilides to 3,4-dihydroquinolin-2(1H)-ones is controlled almost completely by irradiation in a crystalline inclusion compound with an optically active host compound derived from tartaric acid; the configuration of the photocyclisation product is controlled delicately by two hosts with slightly different structures.

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Article type: Paper
DOI: 10.1039/C39920001053
Citation: J. Chem. Soc., Chem. Commun., 1992,0, 1053-1054
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    Control of the stereochemistry in the photocyclisation of acrylanilides to 3,4-dihydroquinolin-2(1H)-ones. Delicate dependence on the host compound

    K. Tanaka, O. Kakinoki and F. Toda, J. Chem. Soc., Chem. Commun., 1992, 0, 1053
    DOI: 10.1039/C39920001053

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