
Tetrahedron Letters p. 2009 - 2010 (1983)
Update date:2022-08-05
Topics:
Ajita, Hiroyuki
Koshiji, Hiroko
Furuichi, Akiya
Horikoshi, Koki
Oishi, Takeshi
(-)-Oudemansin (1) was synthesized from the optically active intermediate 10 obtained by microbiological asymmetric reduction of β-keto ester 3.Oudemansin was found to have the 9S, 10S absolute configuration.
View MoreShanghai Rainbow Chemistry Co., Ltd.
Contact:+86-21-64968086-5815/5812
Address:3rd floor, Building 7, 251 Faladi Road, Zhangjiang Hi-Tech Park, Pudong District, Shanghai, P.R. China
Improve Medical Technology(Nanxiong) Co., Ltd
Contact:86-751-3836997
Address:No.33, Pingan First Road, Fine Chemical Industry Base, Nanxiong City, Shaoguan, Guangdong, China
Jinan Yufeng Bioengineering Co., Ltd.
Contact:+86-531-83130545/83130528/83130525/83130505
Address:Rm415,Building2,No19,Huaneng Road,Jinan, Shandong, China
NINGBO YINLIANG FOREIGN TRADE CO., LTD.
Contact:+86-574-87834016 / 87898057
Address:23F NO.666JINYU ROAD,YINGZHOU DISTRICT,NINGBO.CHINA
Shanghai Mintchem Development ., Ltd
Contact:0086 21 5190 8570
Address:R602,4#,89Nong, Mudan Road Pudong Shanghai China
Doi:10.1039/c4ra00048j
(2014)Doi:10.1021/jo00206a037
(1985)Doi:10.1021/om700454p
(2007)Doi:10.1002/ejic.200600366
(2006)Doi:10.1016/S0040-4039(01)81394-0
(1984)Doi:10.1021/ja01246a025
(1943)