Welcome to LookChem.com Sign In|Join Free

Article Doi

Home > Free PDF Article > 72401-89-9_10.1248/cpb.37.315

Synthesis and biological evaluation of optically active 3-H-1 carbacephem compounds

DOI: 10.1248/cpb.37.315

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 315 - 321 (1989)

Update date:2022-08-02

Topics:

Authors:

Ogasa Ogasa

Saito Saito

Hashimoto

Sato Sato

Hirata Hirata

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

Article abstract of DOI:10.1248/cpb.37.315

View More

Full text of DOI:10.1248/cpb.37.315

NII-Electronic Library Service

NII-Electronic Library Service

NII-Electronic Library Service

NII-Electronic Library Service

NII-Electronic Library Service

NII-Electronic Library Service

NII-Electronic Library Service

Products guided by the article

Product name:(4S*,6R*,7S*)-7-phenylacetamido-4-methyl-8-oxo-1-azabicyclo<4.2.0>oct-2-en-2-carboxylic acid

Cas No:72401-89-9

72401-89-9

R&D Labs maybe for 72401-89-9

Jiaozuo Zhongwen Trading Coporation Limited

Contact:--

Address:East Renmin Road
Synchemie Co., Ltd.

website:http://www.synchemie.com/

Contact:+86-574-87642758

Address:Room 901, Yinyi Bund Building， 132 Renmin Road
Aminodiscovery Co.,Ltd.

Contact:+86-535-8888888

Address:No.161 Haishi Rd.
Jiangsu Feymer Technology Co., Ltd.

Contact:+86-512-58110132

Address:Fenghuang Town, Zhangjiagang City, Jiangsu Province, China
Tianjin Realet Chemical Technology Co.,Ltd.

website:http://www.realetchem.com

Contact:+86-022-58788819

Address:shuanggang industrial park

Relevant to this article

Supramolecular catalysis of Strecker reaction in water under neutral conditions in the presence of β-cyclodextrin

Doi:10.1021/jo052510n
(2006)
Doi:10.1021/ja01026a082
(1968)
Indium-mediated reformatsky-type reaction of β-aminovinyl chlorodifluoromethyl ketones with heteroaryl aldehydes

Doi:10.1055/s-2002-35618
(2002)
A sustainable water-tolerant catalyst with enhanced Lewis acidity: Dual activation of Cp₂TiCl₂ via ligand and solvent

Doi:10.1016/j.mcat.2020.111247
(2020)
Quantitative evaluation of the factors contributing to the copper effect in the stille reaction

Doi:10.1021/om020896b
(2003)
Enantiocomplementary preparation of (S)- and (R)-1-pyridylalkanols via ketone reduction and alkane hydroxylation using whole cells of Pseudomonas putida UV4

Doi:10.1016/S0957-4166(02)00634-1
(2002)

Hot Product

About us - Payment - Contact us - Links - Help Center - Disclaimer
SiteMap | Manufacturers | VIP Product | Suppliers | CAS | New CAS | Cas Database | Article Data | Chemical Catalog | Product Name

©2008 LookChem.com,License:ICP NO.:Zhejiang16009103 complaints:service@lookchem.com
[Hangzhou]86-0571-87562588,87562578,87562573 Our Legal adviser: Lawyer