Addition of sulfonyl chlorides to acetylenes. I. Stereoselective syntheses of. beta.-chlorovinyl sulfones
Y Amiel
Index: Amiel,Y. Journal of Organic Chemistry, 1971 , vol. 36, p. 3691 - 3696
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Citation Number: 40
Abstract
The copper-catalyzed addition of sulfonyl chlorides to acetylenes makes possible the one- step syntheses of p-chlorovinyl sulfones in high yields. The stereoselective 1: 1 addition apparently takes place by a free-radical chain reaction in which the copper catalyst functions as a chlorine atom transfer agent. The stereochemical course of the addition and configurational assignments of the isomeric adducts are discussed. Addition products of ...
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