Journal of Organic Chemistry p. 2930 - 2934 (1985)
Update date:2022-08-04
Topics:
Lenz, Bodo G.
Regeling, Hendrik
Rozendaal, Hendrik L. M. van
Zwanenburg, Binne
The reaction of some α-methylene ketones 1 with thionyl chloride leads to α-oxo sulfines 3 provided the ketone is sufficiently enolized.The reaction of trimethylsilyl enol ethers 2 is a more efficient and versatile method for the synthesis of α-oxo sulfin
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Doi:10.1021/jo00218a019
(1985)Doi:10.1016/0022-2860(95)08902-8
(1995)Doi:10.1002/ardp.19642970303
(1964)Doi:10.1021/ic049746e
(2004)Doi:10.1021/jo00216a036
(1985)Doi:10.1016/S0040-4039(00)86931-2
(1982)
