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 MoreZHANGJIAGANG FREE TRADE ZONE YONG HAN INTERNATIONAL TRADING CO., LTD(expird)
Contact:86 512 57910558
Address:qianjin M road
Wuhan Benjamin Pharmaceutical Chemical Co.,Ltd
Contact:86-27-52341789
Address:Room 1518 B suite, optical valley time square, No 111 Guanshan Road, Hongshan District,Wuhan,Hubei Province,China.
Wuhan Better Organic Technology Inc.
Contact:13307163183
Address:Wuhan Economic&Technology Development Zone, Hubei
Tianjin Emulsion Science&Technology Development Co.,Ltd
Contact:13901380442
Address:Vake Garden New Town New Yi Bai Road Beichen District Tianjin,China
Contact:+91 9963263336
Address:Plot#146A, IDA Mallapur, Hyderabad - 500072
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)
