A SIMPLE PREPARATION OF R OR S GLYCIDIC ESTERS; APPLICATION TO THE SYNTHESIS OF ENANTIOMERICALLY PURE α-HYDROXYESTERS

DOI: 10.1016/S0040-4039(00)96028-3

Source and publish data:

Tetrahedron Letters p. 1993 - 1996 (1987)

Update date:2022-07-31

Topics:

Authors:

Larcheveque, Marc

Petit, Yves

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

Article abstract of DOI:10.1016/S0040-4039(00)96028-3

The simple preparation of enantiomerically pure α-hydroxyesters by the regioselective reaction of lithio and magnesiocuprates with glycidic esters 3 or 3' readily available from serine is described.

Full text of DOI:10.1016/S0040-4039(00)96028-3

Products guided by the article

Product name:Propanoic acid, 2-bromo-3-hydroxy-, (R)-

Cas No:110994-91-7

R&D Labs maybe for 110994-91-7

NanJing Rate Biochemicals CO., LTD

Contact:+86-25-84931986

Address:NO. 1 Hongjing Road,Jiangning Science Park,Nanjing,China
Zibo Xiaoguang Chemical Material Co., Ltd

Contact:15954099116

Address:Boshan Development Zone
Changsha Yonta Industry Co., Ltd.

Contact:+ 86-731-8535 2228

Address:Rm.1717, North Bldg., No.368, East 2nd Ring Road(2nd Section)
Shanxi Tongji Pharmaceuticals Co., Ltd.

Contact:+86-359-3024784

Address:Xikuang South Road, Ruicheng County , Shanxi
Tianjin Pharmacn Medical Technology Co.,Ltd.

Contact:86-22-60122566ext.866(English),23359620

Address:Green Industrial Base, 6 Haitaifazhan Sixth Rd., Huayuan Industrial Area, Tianjin, 300384, China

Relevant to this article

Lewis acid induced homoallylic C-alkylation. A new approach to C-glycosides

Doi:10.1021/jo00235a008
(1987)
Doi:10.1039/jr9570002334
(1957)
Total synthesis of FR901483

Doi:10.1021/ol802870c
(2009)
Catalytic hydrogenation of aromatic rings catalyzed by Pd/NiO

Doi:10.1039/c3ra45600e
(2014)
Lewis Acid Mediated Condensation of Alkenols and Aldehydes. A Selective Synthesis of Tetrahydropyrans and Oxepanes

Doi:10.1021/jo00239a053
(1988)
Crystal structure and third order nonlinear optical studies on 2-phenylbenzimidazolium-p-toulenesulphonate

Doi:10.13005/ojc/340116
(2018)

Article Doi