Regioselectivity in the formation of cyclic sulphones from 4- and 5-alkenesulphonyl chlorides

Peter N. Culshaw*, John C. Walton

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

15 Citations (Scopus)

Abstract

Alk-4-enesulphonyl chlorides and alk-5-enesulphonyl chlorides cyclise under free radical conditions mainly in the endo mode to give tetrahydrothiopyran-1,1-dioxide and thiepane- 1,1-dioxide respectively.

Original languageEnglish
Pages (from-to)6433-6436
Number of pages4
JournalTetrahedron Letters
Volume31
Issue number44
DOIs
Publication statusPublished - 1 Jan 1990

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