Tetrahedron Letters p. 5047 - 5050 (1982)
Update date:2022-08-03
Topics:
Solladie, Guy
Greck, Christine
Demailly, Gilles
Solladie-Cavallo, Arlette
It is shown that reductions of β-ketosulfoxides of identical chirality (R) at sulfur, lead to reduction products of opposite stereochemistry according to the reducing agent used.The high enantiomeric excesses obtained (80 to 100percent) provide a general route to both enantiomers of methylcarbinols from the corresponding esters.
View MoreShanghai Mio Chemical Co., Ltd
Contact:0086 21- 64401188-622
Address:16 Floor NO.2 Jiefang Building, No. 4855 Dushi Road, 201100 Shanghai, P.R.China
Shangyu Sanhechemicals Co.,LTD.
Contact:86-0571-56696839
Address:Num.2952,Nanhuan Road,Binjiang District,Hangzhou,China
Hubei Xiangxi Chemical Industry Co.,Ltd
Contact:+86-710-3454830
Address:No.7, Daqing East Road, Xiangfan City, Hubei Province, China
ZHUHAI HAIRUIDE BIOSCIENCE AND TECHNOLOGY CO.,LTD
website:http://www.zhhairuide.com
Contact:+8613326687259/+86-756-7789199
Address:No.10 Yonghui Road
Qingdao Kingway Pharmtech Co., Ltd.
Contact:86-532-87118899
Address:No. 88, Middle Haixi Road, Jiaonan City, Qingdao, China
Doi:10.1515/znb-2007-0509
(2007)Doi:10.1039/C39790000419
(1979)Doi:10.1016/j.bmc.2004.03.054
(2004)Doi:10.1021/acs.orglett.1c00238
(2021)Doi:10.1016/j.carbpol.2013.04.049
(2013)Doi:10.1021/ja031549b
(2004)
