Tetrahedron Letters p. 1337 - 1340 (1997)
Update date:2022-08-05
Topics:
Connolly, Terrence J.
Durst, Tony
A re-examination of a previously thought general synthesis of sultines from δ-hydroxy sulfoxides is shown to be more complicated than originally believed. The products obtained can be α,α'-dihaloxylenes or δ-halosulfones. The results are best interpreted based on carbocation stability of the key oxo-sulfoxonium salt intermediate.
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Doi:10.1002/hlca.19680510513
(1968)Doi:10.1021/om9607107
(1997)Doi:10.1016/S0040-4020(97)00107-5
(1997)Doi:10.1021/jm9608671
(1997)Doi:10.1039/a603699f
(1997)Doi:10.1021/jo970380f
(1997)
