Studies on synthetic drugs. II. Syntheses of pyrrolol[1,2 d][1,4] benzodiazepine derivatives (Japanese)

DOI: 10.1248/yakushi1947.97.2_135

Source and publish data:

Yakugaku Zasshi/Journal of the Pharmaceutical Society of Japan p. 135 - 142 (1977)

Update date:2022-08-04

Topics:

Authors:

Yamawaki

Watanabe

Yamamura

Saito Saito

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

Article abstract of DOI:10.1248/yakushi1947.97.2_135

Full text of DOI:10.1248/yakushi1947.97.2_135

NII-Electronic Library Service

Products guided by the article

Product name:7-acetyl-10-chloro-11b-phenyl-1,2,7,11b-tetrahydro-benzo[f]pyrrolo[1,2-d][1,4]diazepine-3,6-dione

Cas No:63205-13-0

R&D Labs maybe for 63205-13-0

ZHIJIANG ZENVA SINO COMMERCE AND TRADE CO., LTD.

website:http://www.zenvasino.com

Contact:+86-138-72658998

Address:Shibeishan Road,Zhijiang, Hubei, China
Hangzhou Mole's Science & Technology Co.,Ltd.(expird)

Contact:+86-571-56880228

Address:15F Guodu development Building, NO.182 Zhaohui Road
Chen jie

Contact:027-87677569

Address:Room 2203, yujingmingmen Buidling One, xiongchu Road, wuhan city, hubei province, China
ZHANGJIAGANG FREE TRADE ZONE YONG HAN INTERNATIONAL TRADING CO., LTD(expird)

Contact:86 512 57910558

Address:qianjin M road
Jinhua Haoyuan Chemical CO., LTD(expird)

Contact:86-579-82465583

Address:Jinhua,Zhejiang

Relevant to this article

Decoupled Roles for the Atypical, Bifurcated Binding Pocket of the ybfF Hydrolase

Doi:10.1002/cbic.201300085
(2013)
Doi:10.1021/ja01876a007
(1939)
Design, synthesis and biological evaluation of novel pyridine derivatives as anticancer agents and phosphodiesterase 3 inhibitors

Doi:10.1016/j.bmc.2009.06.063
(2009)
Cinchona alkaloid derived ligands in catalytic asymmetric transfer hydrogenation

Doi:10.1039/b304060g
(2003)
Cationic Chiral Fluorinated Oxazaborolidines. More Potent, Second-Generation Catalysts for Highly Enantioselective Cycloaddition Reactions

Doi:10.1021/jacs.6b00100
(2016)
Doi:10.1016/S0022-328X(00)92039-4
(1977)

Article Doi