Synthesis and structure determination of isomeric 7- and 8-chloro-1,5-benzodiazepine derivatives

DOI: 10.1002/jhet.5570250151

Source and publish data:

Journal of Heterocyclic Chemistry p. 305 - 310 (1988)

Update date:2022-07-30

Topics:

Authors:

Pennini Pennini

Cerri Cerri

Tajana Tajana

Nardi Nardi

Giordano

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

Article abstract of DOI:10.1002/jhet.5570250151

Full text of DOI:10.1002/jhet.5570250151

Products guided by the article

Product name:7-chloro-1,3-dihydro-4-phenyl-2H-1,5-benzodiazepine-2-thione

Cas No:117290-51-4

R&D Labs maybe for 117290-51-4

Dongtai Xinyuan Chemical Co., Ltd.

Contact:+86-21-56733000

Address:404F, 99Nong No.117 Zhongtan Rd. Shanghai
Mollt Biochem Co., Ltd(expird)

Contact:+86-21-38682181

Address:shanghai ,china
shanghai jinshan pharmaceutical Co.,Ltd

Contact:021-57363011，13681638167

Address:No. 7966 Tingfeng Road,Jinshan,Shanghai,China
Wuhan Yitongtai Science and Technology Co.,Ltd.

Contact:+86-27-88933550

Address:27th Fl. Bldg. 1, Shuian International Mansion, Heping Ave, Wuhan, Hubei, China
Zouping Mingxing Chemical Co.,Ltd.

website:http://www.zoutong.com.cn

Contact:86-543-2240068 2240067

Address:428 Daixi Third Road Zouping County Shandong Province China

Relevant to this article

SYNTHESIS OF A POTENT ANTITHROMBIN ACTIVATING PENTASACCHARIDE: A NEW HEPARIN LIKE FRAGMENT CONTAINING TWO 3-O-SULPHATED GLUCOSAMINES

Doi:10.1016/S0040-4039(00)80214-2
(1988)
Structure-activity relationships and cancer-cell selective toxicity of novel inhibitors of glioma-associated oncogene homologue 1 (Gli1) mediated transcription

Doi:10.1021/jm900106f
(2009)
An efficient and facile synthesis of pyrimidine and quinazoline derivatives via one-pot three-component reaction under solvent-free conditions

Doi:10.1002/jhet.43
(2009)
Lipase-catalyzed highly enantioselective kinetic resolution of boron-containing chiral alcohols

Doi:10.1021/ol901091f
(2009)
Methyleneimidazoline complexes of iridium, rhodium, and palladium from selective C(sp³)-H bond activation

Doi:10.1002/chem.200802569
(2009)
Original and efficient synthesis of 2:1-[α/aza]-oligomer precursors

Doi:10.1016/j.tetlet.2009.04.131
(2009)

Article Doi