Chemical Communications p. 2745 - 2746 (1996)
Update date:2022-08-28
Topics:
Kashiwagi, Yoshitomo
Yanagisawa, Yoshinori
Kurashima, Futoshi
Anzai, Jun-Ichi
Osa, Tetsuo
Bobbitt, James M.
The S-isomers of four racemic sec-alcohols, which possess a chiral centre at the α-position to the hydroxy group, were oxidized to the corresponding ketones whereas the R-isomers remained unreacted on a TEMPO-modified graphite felt electrode in the presence of (-)-sparteine, where the enantiopurity of the remaining R-isomers was >99% and the current efficiency for the produced ketones was >90%.
View MoreShanghai Forever Biotech Co., Ltd.
Contact:+86-21-69734790
Address:Room 5017/5019、5022、5024 of Technology Innovation Centre, No.1155, Gongyuan East Rd, QingPu District, Shanghai China.
Jinan Jinguilin Chemical Co.,Ltd
Contact:+86-531-81188412
Address:3rd floor of Torch Building, Huanyuan Rd, City of Jinan
Beijing Top Science biological technology co., LTD
Contact:+86-13439059536
Address:15-1705 jre three mile, Beijing 100000,CHINA
Laohekou Jinghong Chemical Co.,Ltd
Contact:+86-0710-3702747
Address:163.East，Huagong Road，Laohekou
Kaymossy BioChem Tech Co., Ltd
website:http://www.kaimosi.com
Contact:0571-87191913/0571-87199097
Address:Room 215, Building 3rd, No.288 Ningxia Road, Qingdao city, China
Doi:10.1016/j.bmc.2017.04.024
(2017)Doi:10.1016/S0022-328X(00)94435-8
(1980)Doi:10.1021/jo00277a049
(1989)Doi:10.1016/0022-1902(59)80225-6
(1959)Doi:10.1021/jo01106a613
(1958)Doi:10.1016/S0957-4166(03)00282-9
(2003)
