Tetrahedron Letters p. 4983 - 4986 (1998)
Update date:2022-08-05
Topics:
Dankwardt, John W.
Dankwardt, Sharon M.
Schlessinger, Richard H.
The synthesis of the C-28 through C-38 segment of the marine natural product okadaic acid was accomplished employing a highly enantio- and diasteroselective aldol condensation reaction of a chiral vinylogous urethane enolate. The stereocenter at C-29 was addressed utilizing a diastereoselective hydroboration reaction.
View MoreGolden Union Agrochemical Import and Export Co., Ltd.
Contact:86-755-23910527
Address:Room 1106, Tower 3A, Excellence Century Center, Futian District, Shenzhen, China
Contact:+86-25-85281586
Address:13F,Bld2#,South of Longpan Road
Shandong Xinke Petrochemical Co., Ltd.
Contact:+86-546-7277016
Address:Gudao Industrial Park, Hekou District, Dongying, Shandong Province, China
Hangzhou Eastbiopharm Co.,Ltd.
Contact:+86-571-88931780
Address:Hangzhou,China
Anhui Dexinjia Biopharm Co., Ltd
Contact:+86-531-82375818
Address:9 Hexie Road, kaifaqu, Taihe
Doi:10.1080/00397919808004880
(1998)Doi:10.1021/ja01183a078
(1948)Doi:10.1021/jo061346g
(2007)Doi:10.1016/S0008-6215(98)00107-4
(1998)Doi:10.1016/S0040-4039(98)01344-6
(1998)Doi:10.1016/S0960-894X(98)00401-6
(1998)
