Tetrahedron Letters p. 3299 - 3302 (1985)
Update date:2022-08-05
Topics: Synthesis NMR spectroscopy Chiral Catalyst Enantioselective Isolation HPLC (high-performance liquid chromatography) Enantiomeric excess Reaction Conditions Chiral Auxiliary Degradation product Carzinophilin
Garner, Philip
Park, Jung Min
Rotello, Vicent
An efficient, enantioselective synthesis of (2S,3S) 4-amino-2,3-dihydroxy-3-methylbutyric acid (1) is described.The sequence includes the direct use of azide to selectively open a secondary epoxy alcohol formed under Payne rearrangement conditions.
View MoreBeijing Cooperate Pharmaceutical Co.,Ltd
website:http://www.cooperate-pharm.com/
Contact:86-01060279497
Address:No.507,Building 4,Tianhua Street, Biomedicine industrial Base
Linyi Shengxin Pharmaceutical R&D Co., Ltd
Contact:+86-18653953873
Address:West First of Yufeng Road, Yishui County
Contact:+852 83038667
Address:Room 1502, 15th Floor, SPA Centre,53-55 Lockhart Road, Wanchai, Hong Kong
Hangzhou jls Flame Retardants Chemical Co.,Ltd
Contact:+86-571-87250387/87250386
Address:MOGANSHAN RODA 1418# SHANGCHENG INDUSTRIAL PARK
Xi'an Kaixiang Photoelectric Technology Co., Ltd
website:http://www.kxmaterials.com/
Contact:86-29-15991651477
Address:Building 6, Biopharmaceutical Industry R&D Cluster Base, No. 16, Caotang 4th Road, Caotang Science and Technology Industrial Base, High-tech Zone, Xi'an City, Shaanxi Province, China
Doi:10.1021/ol702929k
(2008)Doi:10.1021/jm801421q
(2009)Doi:10.1016/j.tetlet.2007.12.018
(2008)Doi:10.1055/s-0031-1289304
(2011)Doi:10.1093/gerona/56.4.M243
(1958)Doi:10.1021/jo01117a017
(1956)
