Synthesis of 5H-tetrazolo[5,1-c][1,4]benzodiazepines

DOI: 10.1002/jhet.5570220221

Source and publish data:

Journal of Heterocyclic Chemistry p. 333 - 336 (1985)

Update date:2022-08-05

Topics:

Authors:

Klaubert

Bell Bell

Pattison

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

Article abstract of DOI:10.1002/jhet.5570220221

Full text of DOI:10.1002/jhet.5570220221

Products guided by the article

Product name:Benzene, 2-(azidomethyl)-4-chloro-1-nitro-

Cas No:95668-82-9

R&D Labs maybe for 95668-82-9

Wuxi Morality Chemical Co., Ltd(expird)

Contact:

Address:B/7F, 321th WuYun Rd, Wanda Plaza, Wuxi City, 214174, China
Shuanghe Bio-Technology Limited(expird)

Contact:+86-571-61710758,18968016640

Address:Jinqiao north road 916# Fuyang
Nantong Chem-land Co., Ltd.

Contact:86 513 85512619

Address:Rm.1306, Building A, Wenfeng Mansion,168 Gongnong Road, Nantong Jiangsu China
Suzhou Howsine Biological Technology Co.,Ltd(expird)

website:http://www.howsine.com

Contact:86-512-67262751

Address:No 3,Weihua Road ,Suzhou Industrial Park ,Jiangsu ,China.
QUZHOU ZIO I/E CO.;LTD

Contact:13357117572

Address:No.149 Shiji dadao Road.

Relevant to this article

REACTIONS INVOLVING FLUORIDE ION. PART 31. CO-OLIGOMERS OF PERFLUORO-1-METHYL-1,3-DIAZACYCLOPENT-2- AND -3-ENE

Doi:10.1039/P19850000053
(1985)
THE SYNTHESIS OF 1H-PYRAZOL-4-OLS FROM 2-(2-ALKYLIDENEHYDRAZINO)ACETIC ACIDS

Doi:10.1016/S0040-4039(00)80291-9
(1988)
Solvent-controlled copper-catalyzed oxidation of benzylic alcohols to aldehydes and esters

Doi:10.1002/ejoc.201300668
(2013)
Enhanced brightness emission-tuned nanoparticles from heterodifunctional polyfluorene building blocks

Doi:10.1021/ja311497e
(2013)
Synthesis of highly hindered 1,2-diaryl diketones and of cis- and trans-1,2-diacetoxy-1,2-bis(aryl)ethenes

Doi:10.1039/a809045i
(1999)
Benzyl 1,2,3,5,11,11a-hexahydro-3,3-dimethyl-1-oxo-6H-imidazo[3′,4′:1,2]pyridin[3,4-b]indole-2-substituted acetates: One-pot-preparation, anti-tumor activity, docking toward DNA and 3D QSAR analysis

Doi:10.1016/j.bmc.2010.01.038
(2010)

Article Doi