Highly regioselective ring opening of epoxides and aziridines using (bromodimethyl) sulfonium bromide
B Das, M Krishnaiah, K Venkateswarlu
Index: Das, Biswanath; Krishnaiah, Maddeboina; Venkateswarlu, Katta Tetrahedron Letters, 2006 , vol. 47, # 26 p. 4457 - 4460
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Citation Number: 44
Abstract
Epoxides and aziridines undergo ring opening efficiently with (bromodimethyl) sulfonium bromide at room temperature to form the corresponding β-bromohydrins and β- bromoamines, respectively. The conversions are highly regioselective and afford the products in excellent yields within a short period of time.
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