Diastereoselective cyclization of a dithienylethene switch through single crystal confinement

Org Biomol Chem. 2006 Mar 21;4(6):1002-6. doi: 10.1039/b517370a. Epub 2006 Feb 10.

Abstract

Upon UV irradiation of the hydrogen-bond confined crystal state of a dithienylhexafluorocyclopentene with (R)-N-phenylethylamide substituents, the photochemical cyclization reaction proceeds diastereoselectively to form the coloured, closed-ring isomer with 97% de.