Abstract
AbstractA copper-catalyzed construction of isothiochromenes and benzo[b]thiophenes via annulation with 1,1,1,3,3,3-hexamethyldisilathiane as a sulfur source is described. In the isothiochromene synthesis, the use of the disilathiane as a sulfur source successfully controls the regioselectivity of cyclization to afford the isothiochromene as the sole product. The present strategy can be applied to the synthesis of 2-aryl/2-alkylbenzo[b]thiophenes.
Funder
Japan Society for the Promotion of Science
OGAWA Science and Technology Foundation
Subject
Organic Chemistry,Catalysis
Cited by
3 articles.
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