
Bulletin of the Chemical Society of Japan p. 1767 - 1780 (1987)
Update date:2022-08-03
Topics:
Inomata, Katsuhiko
Sasaoka, Shin-ichi
Kobayashi, Toshifumi
Tanaka, Yuhji
Igarashi, Susumu
et al.
1- or 2-p-Tolylsulfonyl(=tosyl)-1-alkenes, vinylic sulfones, were regioselectively prepared from 1-alkenes via iodosulfonization or sulfonylmercuration and also from 1-haloalkanes by the homologation or unhomologation methods.The vinylic sulfones thus prepared were further converted to the corresponding allylic sulfones under basic conditions.The stereochemistry of this conversion was discussed.One-carbon homologated allylic sulfones were directly obtained from aldehydes in good yields by the reaction with diethyl phenylsulfonylmethylphosphonate and 1,8-diazabicyclo<5.4.0>undec-7-ene (DBU) under mild conditions.
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Doi:10.1246/bcsj.61.2767
(1988)Doi:10.1007/BF00759433
(1987)Doi:10.1080/10426500213423
(2002)Doi:10.1016/0040-4020(72)80075-9
(1972)Doi:10.1515/znb-1964-0507
()Doi:10.1021/jo026605q
(2003)