Regio- and enantio-selective photoreactions of cyclohex-2-enone, coumarin and acrylanilide as inclusion complexes with optically active host compounds

Article abstract of DOI:10.1080/10587259408027161

Regio- and enantio-selective photodimerization reactions of cyclohex-2-enone (4) and coumarin (7), and enantioselective photocyclization of acrylanilides (12, 16, 18, and 20) in inclusion crystal with optically active host compounds (1, 2, and 3) are reported. X-ray structure studies of the inclusion crystal are also reported.

Full text of DOI:10.1080/10587259408027161

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Molecular Crystals and Liquid Crystals
Science and Technology. Section A.
Molecular Crystals and Liquid Crystals
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Regio- and Enantio-Selective
Photoreactions of Cyclohex-2-Enone,
Coumarin and Acrylanilide as Inclusion
Complexes with Optically Active Host
Compounds
Koichi Tanaka a , Fumio Toda a , Yoichi Ueda b & Takaji Fukiwara b
a Department of Applied Chemistry, Faculty of Engineering , Ehime
University , Matsuyama, Ehime, 790, Japan
b Department of Information Science, Faculty of Science , Shimane
University , Matsue, Shimane, 690, Japan
Published online: 24 Sep 2006.
To cite this article: Koichi Tanaka , Fumio Toda , Yoichi Ueda & Takaji Fukiwara (1994) Regio-
and Enantio-Selective Photoreactions of Cyclohex-2-Enone, Coumarin and Acrylanilide as
Inclusion Complexes with Optically Active Host Compounds, Molecular Crystals and Liquid Crystals
Science and Technology. Section A. Molecular Crystals and Liquid Crystals, 248:1, 43-47, DOI:
10.1080/10587259408027161
To link to this article: http://dx.doi.org/10.1080/10587259408027161
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Evaluation Only. Created with Aspose.PDF. Copyright 2002-2021 Aspose Pty Ltd.

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