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
View MoreChangsha Nutritopper Bio Technology Co.,Ltd.
Contact:+86-731-87803543
Address:East 1st Street, Baima Road, Ningxiang County
PINGYUAN SIHUAN PHARMACEUTICAL CO., LTD
Contact:+86-531-55696072
Address:#2766,yinxiu Road, Economic Development Zone, Pingyuan Country, Shandong Province, China.
Contact:+86-570-4336358
Address:No.87 Building,Tianqian,Sidu Town
Pengchen New Material Technology Co., Ltd.
Contact:+86-512-63680537
Address:99.6 km of national road 318, Meiyan Community,Pingwang Town, Wujiang District, Suzhou 215225
Contact:+86-0760-85282375
Address:zhongjing road,zhongshan torch hi-tech industrial development zone
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)
