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 MoreHANGZHOU PANYU CHEMICAL CO.,LIMITED
Contact:+86-571-86578491
Address:Rm 605, NO.1870 Binsheng Road,Binjiang Dist, Hangzhou, China
Taizhou Chemedir Biopharm-tech Co., Ltd
Contact:+86 523 86200218
Address:G09, No. 1 Avenue China Medical City, Taizhou,Jiangsu, China
Contact:+86-20-62802632;62802633
Address:Room 330 GIGCAS Building,No.511 Kehua Street,Tianhe District
Wuhan Konberd Biotech Co., Ltd.
Contact:+86-27-87205925
Address:NO.666, Gaoxin Road, Eastlake High-tech zone
Hangzhou Ocean Chemical Co., Ltd.
website:http://www.hzoceanchem.com
Contact:+86-571-88025872, 28272092, 28272096
Address:Room 623 ,Building No 1 , COFCO Radius Commercial Center Xiwen Road, Xiacheng District, Hangzhou, Zhejiang Province, China
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)
