A stereospecific synthesis of (-)-bestatin from L-malic acid

DOI: 10.1016/S0040-4039(00)61780-X

Source and publish data:

Tetrahedron Letters p. 6803 - 6806 (1992)

Update date:2022-08-04

Topics:

Authors:

Norman Norman

Morris Morris

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1016/S0040-4039(00)61780-X

A highly diastereospecific route to (-)-Bestatin from L-Malic Acid has been developed. This approach features a stereocontrolled alkylation of diethyl (S)-malate and proceeds through an oxazolidone via a Curtius Rearrangement.

Full text of DOI:10.1016/S0040-4039(00)61780-X

Products guided by the article

Product name:(4R,5S)-4-Benzyl-2-oxo-oxazolidine-5-carboxylic acid ethyl ester

Cas No:145872-15-7

R&D Labs maybe for 145872-15-7

C-LAB Chemievermittlung GmbH

Contact:+49-9398-993127

Address:Untertorstr. 27
HANGZHOU GOPHER CHEM-TECH CO.,LTD

Contact:86-189-58111780

Address:Da Cheng Ming Zuo Plaza,Xiaoshan District
Taizhou Chemedir Biopharm-tech Co., Ltd

Contact:+86 523 86200218

Address:G09, No. 1 Avenue China Medical City, Taizhou,Jiangsu, China
DACHANG OLEOCHEMICALS CO.,LTD.

Contact:0543-2875999

Address:Xingbo 10 Road,EDZ,Boxing Town,Shandong
Yingkou Sanzheng Organic Chemical Co. Ltd.

Contact:+86-417-3638818

Address:25 Gengxinli Village, Daqing Road, Yingkou, Liaoning, China

Relevant to this article

Stereoselective synthesis of novel antiproliferative steroidal (E, E) dienamides through a cascade aldol/cyclization process

Doi:10.1016/j.steroids.2013.08.001
(2013)
A novel stereoselective synthesis of substituted γ-butyrolactones

Doi:10.1016/S0040-4039(00)60201-0
(1992)
A total synthesis of dl-Cerulenin

Doi:10.1021/ja00498a032
(1979)
Stereoselective Synthesis of (+/-)-Ancistrofuran and its Stereoisomers

Doi:10.1039/P19850002463
(1985)
Ozonolysis of Trifluoroethylene, 1,1-Difluoroethylene, and Perfluoroethylene. Epoxide and Ozonide Formation

Doi:10.1021/ja00545a035
(1980)
Doi:10.1055/s-1979-28624
(1979)

Article Doi