Chiral 1,2-dithiine as a sulfur rich electron acceptor
Abstract
The selective synthesis of both enantiomers of a Sulfur rich electron acceptor containing two 1-phenylethyl groups of the same chirality and a chiral axis is described. Cyclisation into enantiopure dithiine has been induced by the presence of a chiral substituent on the nitrogen atom of a thiazoline-2-thione dithiolate precursor.
Domains
Chemical Sciences
Origin : Files produced by the author(s)
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