Phenylsulfenyl chloride/N, N-diisopropylethylamine: A useful reagent for cyclic ether formation (sulfenyletherification)
SM Tuladhar, AG Fallis
Index: Tuladhar, Sudersan M.; Fallis, Alex G. Tetrahedron Letters, 1987 , vol. 28, # 5 p. 523 - 526
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Citation Number: 29
Abstract
Abstract A general method for the formation of cyclic ethers and lactones is described. The procedure employs phenylsulfenyl chloride and N, N-diisopropylethylamine to generate an episulfonium ion intermediate from which the cyclic products arise by internal nucleophilic displacement.
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