SYNTHESES D'ESTERS OU D'ACIDES α-HALOGENES A PARTIR DES GEM DICYANO EPOXIDES.

DOI: 10.1016/S0040-4020(01)90607-6

Source and publish data:

Tetrahedron p. 2275 - 2282 (1986)

Update date:2022-07-29

Topics:

Authors:

Robert, A.

Jaguelin, S.

Guinamant, J. L.

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

Article abstract of DOI:10.1016/S0040-4020(01)90607-6

α-halogeno esters or α-halogenoacids were easily prepared by selective one pot reaction of gem-dicyano epoxides with halohydric acids in an alcoholic or aqueous media.

Full text of DOI:10.1016/S0040-4020(01)90607-6

Products guided by the article

Product name:2,2-dicyano, 3-methyl-3-phenyloxirane

Cas No:33441-58-6

R&D Labs maybe for 33441-58-6

Tianjin Anda North Industrial & Business Co.Ltd.

Contact:86-22-24999306

Address:No.11 Erwei Road,Dongli Development Area,Tianjin,China
Xinyanhe Pharmatech Co.,Ltd

Contact:+86-519-8525-2752

Address:Changzhou
zhangjiagang bonded areas banggao co;ltd

website:http://www.shunchangchem.com

Contact:0086-13921972933

Address:Dongsha Chemical Zone.Zhangjiagang, Jiangsu Province
Anhui Gusheng Import&Export CO.,LTD

Contact:86-551-63662296

Address:Jinzhai Road NO.162 ,hefei, china
wuxi huabin bio-tech Co.,Ltd(expird)

Contact:86-0510-85133006

Address:hubin road NO157

Relevant to this article

A new strategy for the stereoselective introduction of steroid side chain via α-alkoxy vinyl cuprates: Total synthesis of a highly potent antitumor natural product OSW-1 [2]

Doi:10.1021/ja004098t
(2001)
Doi:10.1021/jo00973a032
(1972)
A combination of flow and batch mode processes for the efficient preparation of mGlu_2/3 receptor negative allosteric modulators (NAMs)

Doi:10.1016/j.tet.2018.03.068
(2018)
Doi:10.1139/v71-450
(1971)
The Michael Addition of Indole to α,β-Unsaturated Ketones Catalyzed by Iodine at Room Temperature

Doi:10.1055/s-2003-42105
(2003)
Cobalt-Catalyzed Carbon-Carbon Bond Formation via Radicals

Doi:10.1016/S0040-4039(00)61308-4
(1992)

Article Doi