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 language | English |
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Pages (from-to) | 6433-6436 |
Number of pages | 4 |
Journal | Tetrahedron Letters |
Volume | 31 |
Issue number | 44 |
DOIs | |
Publication status | Published - 1 Jan 1990 |