Tetrahedron Letters p. 3479 - 3482 (1982)
Update date:2022-08-04
Topics:
Hoffmann, Reinhard W.
Helbig, Wilfried
Ladner, Wolfgang
Diastereoselective and enantioselective reduction of the β-ketoester 3 by yeast to 4 provided the chiral starting material for a synthesis of 4RS,6S,7S-serricornine, having the same configuration as the natural product.This material was converted into optically active and diastereomerically pure 6S,7S-anhydro-serricornine (2).
View MoreJiangsu Allyrise Pharmaceutical Co., Ltd.(expird)
Contact:+86-523-86818997
Address:Taizhou,Jiangsu Province,CHINA
Yangling Ciyuan biotech Co., Ltd.
Contact:86-15802970736
Address:2-1804, International Park Mansion, No.2, South Fengdeng Road, Lianhu District
Jinan Samuel Pharmaceutical Co., Ltd
Contact:+86 400-652-8886
Address:Room 1106, Building 2, Jinan Pharm Valley 1 North Gangxing Road, Jinan New High-Tech Area Jinan, Shandong China
Contact:+86-371-55981030
Address:Room 1571, Macalline Soho, No.1, Shangdu Road, Zhengzhou, Henan
Beijing Apis Biotechnology Co., Ltd.
Contact:86-010-67856775-8551
Address:NO.4PUHUANGYU ROAD,FENTAI DISTRICT, BEIJING, CHINA
Doi:10.1016/j.chemphyslip.2007.09.007
(2008)Doi:10.1021/jo00200a046
(1984)Doi:10.1016/S0040-4039(01)90195-9
(1984)Doi:10.1016/j.tetasy.2006.12.023
(2007)Doi:10.1021/jo01051a520
(1962)Doi:10.1002/anie.201603260
(2016)
