A simple and highly effective oxidative chlorination protocol for the preparation of arenesulfonyl chlorides

YM Pu, A Christesen, YY Ku

Index: Tetrahedron Letters, , vol. 51, # 2 p. 418 - 421

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Citation Number: 16

Abstract

... Tetrahedron Letters. Volume 51, Issue 2, 13 January 2010, Pages 418–421. ... proceeded smoothly to afford the desired sulfonyl chlorides in good yields (Table 2, entries 1–8). It is noted that no desired product was formed from p-bromophenylmethyl sulfide ( Table 2, entry 9 ...