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Chiral helicenoid diarylethene with highly diastereoselective photocyclization. | LitMetric

Chiral helicenoid diarylethene with highly diastereoselective photocyclization.

J Org Chem

Department of Advanced Materials Chemistry, Graduate School of Engineering, Yokohama National University, Hodogaya, Yokohama 240-8501, Japan.

Published: March 2007

A novel photochromic helicenoid diarylethene (R)-1-[1-(1-methoxymethoxyethyl)-2-naphtho[2,1-b]thienyl]-2-(2,4,5-trimethyl-3-thienyl)hexafluorocyclopentene was synthesized enantioselectively. It showed highly diastereoselective photocyclization (90% de) and a large change (950 degrees) in the specific optical rotation value at 633 nm upon UV light irradiation in ethyl acetate.

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http://dx.doi.org/10.1021/jo062022vDOI Listing

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