Journal
TETRAHEDRON LETTERS
Volume 49, Issue 45, Pages 6471-6474Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2008.08.109
Keywords
Ring-opening reaction; Ionic liquid; beta-Hydroxy selenide; beta-Hydroxy sulfide
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Funding
- National Natural Science Foundation of China [204720280]
- Natural Science Foundation of Zhejiang Province [Y407081]
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A Regioselective ring-opening reactions of 1,2-epoxides with ArSH and ArSeH promoted by ionic liquid [Bmim]BF4 were investigated. A variety of beta-hydroxy selenides and beta-hydroxy sulfides were obtained in excellent yields (81-99%) with good regioselectivities using a mild, simple and environmentally benign procedure. (C) 2008 Elsevier Ltd. All rights reserved.
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