A unified strategy for exceptionally high diastereoselectivity in the photochemical ring closure of chiral diarylethenes.

Angew Chem Int Ed Engl

Department of Advanced Materials Chemistry, Yokohama National University, Tokiwadai, Hodogaya, Yokohama 240-8501, Japan.

Published: July 2009

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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http://dx.doi.org/10.1002/anie.200901156DOI Listing

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