Penicillin-cephalosporin conversion. XII. Electroreductive dechlorination of 3'-chlorocephalosporins into 3-methylenecephams

DOI: 10.1246/bcsj.59.3975

Source and publish data:

Bulletin of the Chemical Society of Japan p. 3975 - 3976 (1986)

Update date:2022-08-05

Topics:

Authors:

Torii Torii

Tanaka Tanaka

Ohshima Ohshima

Sasaoka Sasaoka

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

Article abstract of DOI:10.1246/bcsj.59.3975

Full text of DOI:10.1246/bcsj.59.3975

Products guided by the article

Product name:(6R)-3-methyl-8-oxo-7t-(2-phenyl-acetylamino)-(6rH)-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzyl ester

Cas No:34708-39-9

R&D Labs maybe for 34708-39-9

Wuhan Soleado Technology Co.,Ltd.

Contact:86-2783341481 18971291927

Address:RM2405 Unit 1 Builing 1, Taiyin Tower, Changqing Road,Wuhan China
Jining Shengrun Chemical Industry Co., Ltd.

Contact:+86-537-7121666 ,

Address:West Ring Road,Wenshang County Shandong Province
Yuan Shi(SuQian)Biotechnology Co.,Ltd

website:http://www.yuanshibio.com

Contact:+86-527-84226672

Address:jiangsu suqian
Chinapeptides Co,. Ltd

Contact:+86-021-50792271

Address:Building 24A, 300 Chuantu Road, Chuansha, Pudong new area, Shanghai, China, 201202
Hangzhou Eastbiopharm Co.,Ltd.

Contact:+86-571-88931780

Address:Hangzhou,China

Relevant to this article

Doi:10.1021/jo01283a029
(1967)
Antineoplastic Agents. 585. Isolation of Bridelia ferruginea Anticancer Podophyllotoxins and Synthesis of 4-Aza-podophyllotoxin Structural Modifications

Doi:10.1021/acs.jnatprod.5b00873
(2016)
Sphingomyelin analogues as inhibitors of sphingomyelinase

Doi:10.1016/S0960-894X(03)00360-3
(2003)
ASYMMETRIC SYNTHESIS OF CYCLOALIPHATIC α-AMINO ACIDS WITH A NORBORNANE SKELETON

Doi:10.1016/0957-4166(90)90038-C
(1990)
A Novel Palladium-Catalyzed Intramolecular Redox Reaction

Doi:10.1021/ol015813m
(2001)
Syntheses, crystal structures, and solid-state spectroscopic properties of helical and non-helical dinuclear zinc(II) complexes derived from N₂O₂ ligands with different torsion-generating sources

Doi:10.1016/j.ica.2019.118979
(2019)

Article Doi