FORMATION OF α,β-EPOXY SYSTEMS FROM β-PEROXY CARBON FREE RADICALS

DOI: 10.1016/S0040-4039(00)88126-5

Source and publish data:

Tetrahedron Letters p. 3169 - 3170 (1983)

Update date:2022-08-06

Topics:

Authors:

Corey, E. J.

Schmidt Greg

Shimoji Katsuichi

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

Article abstract of DOI:10.1016/S0040-4039(00)88126-5

The conversion of β-peroxy carbon free radicals to α,β-epoxides is a facile process of broad scope and may be a key step in the biosynthesis of clavulones.

Full text of DOI:10.1016/S0040-4039(00)88126-5

Products guided by the article

Product name:trans-1-(3-methyloxiranyl)-ethanone

Cas No:105926-97-4

R&D Labs maybe for 105926-97-4

JADECHEM NINGBO CO.,LTD.

Contact:+86-574-89075960

Address:#100 Xiang Yun Road, New High tech area, Ningbo, China
Jinan Decheng Hemu Medical Technology Co.，Ltd.

Contact:+86-531-68650525

Address:NO.554 Zhengfeng Road High-new Technology Development Zone
Shanghai Sunway Pharmaceutical Technology Co.,Ltd.

Contact:+86-21-5161 3915

Address:Shanghai YangPu
Jurong Huaheng Natural Biological Products Factory

website:http://www.risebiochem.com

Contact:+86-13921007726

Address:Chuncheng town,Jurong city,Jiangsu province,China
Shochem(Shanghai) Co., Ltd

website:http://www.shochem.com

Contact:021-50800795

Address:No.1043, Halei Rd, Zhangjiang Hi-Tech Park, Shanghai, Postcode 201203, China

Relevant to this article

1,8-Naphthyridines VII. New substituted 5-amino[1,2,4]triazolo[4,3-a][1,8]naphthyridine-6-carboxamides and their isosteric analogues, exhibiting notable anti-inflammatory and/or analgesic activities, but no acute gastrolesivity

Doi:10.1016/j.ejmech.2007.10.010
(2008)
Synthesis of Sydnone Compounds Substituted by Heteroatom Groups at the 4-Positions

Doi:10.1246/bcsj.59.483
(1986)
Reactions with β-Cyanoethylhydrazine, III A New Approach for the Synthesis of Substituted 3,5-Diaminopyrazole and 1,2,4-Triazoles

Doi:10.1007/BF00809440
(1986)
Synthesis of potential Rho-kinase inhibitors based on the chemistry of an original heterocycle: 4,4-Dimethyl-3,4-dihydro-1H-quinolin-2-one

Doi:10.1016/j.ejmech.2007.11.010
(2008)
Enantioselective Henry reaction catalyzed by Cu^II salt and bipiperidine

Doi:10.1021/jo902664v
(2010)
Study of chemical stability of antivirally active 5-azacytosine acyclic nucleoside phosphonates using NMR spectroscopy

Doi:10.1016/j.bmc.2008.05.058
(2008)

Article Doi