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A Unified Strategy for Exceptionally High Diastereoselectivity in the Photochemical Ring Closure of Chiral Diarylethenes
Authors:Yasushi Yokoyama Prof. Dr.  Tatsuya Shiozawa  Yutaka Tani Dr.  Takashi Ubukata Dr.
Affiliation:Department of Advanced Materials Chemistry, Yokohama National University, Tokiwadai, Hodogaya, Yokohama 240‐8501 (Japan), Fax: (+81)?45‐339‐3934, http://www.chem.ynu.ac.jp/lab/yokoyamalab/public_html/home‐E.html
Abstract:Into my arms : Photochemical cyclization of diarylethenes that have two chiral side arms showed up to 100 % de (see scheme). Introduction of these chiral side arms onto the carbon atoms where ring closure occurs is a general strategy for the highly diastereoselective cyclization of diarylethenes.
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Keywords:diastereoselectivity  electrocyclization  photochromism
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