Quinazolines and 1,4-benzodiazepines. XC(1). 2-aminoimidazo[1,5 a][1,4]benzodiazepin-1-ones and derivatives

DOI: 10.1002/jhet.5570170810

Source and publish data:

Journal of Heterocyclic Chemistry p. 1697 - 1699 (1980)

Update date:2022-09-26

Topics:

Authors:

Walser Walser

Flynn Flynn

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

Article abstract of DOI:10.1002/jhet.5570170810

Full text of DOI:10.1002/jhet.5570170810

Products guided by the article

Product name:

Cas No:77563-66-7

R&D Labs maybe for 77563-66-7

Jinan Finer Chemical Co., Ltd

website:http://www.finerchem.com

Contact:+86-531-88989536

Address:New Material Industry Park, Jinan Ciyt, China
Synchem Pharma Co.,Ltd(expird)

Contact:+0086-21-61984905-1

Address:Building 60,Zimian Park, LongYang industrial Area, 1515Nong，Yuandong Road Fengxian District, Shanghai ,China
Ji'an Kexin Trade Co., Ltd.(expird)

Contact:86-0796-8187704 18507063190

Address:ji'an jiangxi
Changsha Kamer Essence and Flavor Co.,Ltd

Contact:86-731-89832270

Address:No.327 Kangnin Road Changsha Bio Information Industry Park, Changsha city, Hunan province
Maithili Life Sciences

Contact:+91 9963263336

Address:Plot#146A, IDA Mallapur, Hyderabad - 500072

Relevant to this article

Fluoro-substituted phenylazocarboxamides: Dopaminergic behavior and N-arylating properties for irreversible binding

Doi:10.1016/j.bmc.2014.12.012
(2015)
A formal total synthesis of salvadione

Doi:10.1002/ejoc.200600361
(2006)
Photostable BODIPY-based molecule with simultaneous type i and type II photosensitization for selective photodynamic cancer therapy

Doi:10.1039/c3tb21547d
(2014)
Synthesis of heterocyclic α-aminophosphonic acids

Doi:10.1080/00397919408011729
(1994)
Highly selective and controllable synthesis of arylhydroxylamines by the reduction of nitroarenes with an electron-withdrawing group using a new nitroreductase BaNTR1

Doi:10.1039/c3cc48590k
(2014)
N-metallacycles from [CpMX₂]₂ and alkynylpyridines: Synthesis, reaction pathway, and aromaticity

Doi:10.1021/om401154c
(2014)

Article Doi