Attempted synthesis of 1,4-benzodiazepine comprising an additional ring at the 1-3 position

DOI: 10.1002/jhet.5570130322

Source and publish data:

Journal of Heterocyclic Chemistry p. 529 - 532 (1976)

Update date:2022-09-26

Topics:

Authors:

Klein Klein

Golik Golik

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

Article abstract of DOI:10.1002/jhet.5570130322

Full text of DOI:10.1002/jhet.5570130322

Products guided by the article

Product name:Butanoic acid, 3-(benzoylamino)-4-[(4-chlorophenyl)amino]-, ethyl ester

Cas No:60655-95-0

R&D Labs maybe for 60655-95-0

Chengdu Push Bio-technology Co., Ltd

Contact:86-28-85370565

Address:No.8 Wuke West Second Road, Wuhou
X.T.Y Environ-Tech Co.,Ltd

Contact:+86-310-7092106

Address:Quzhou Modern & New Industrial Park, Handan, Hebei 057250, China
Shanghai Longjin Metallic Material Co., Ltd.

website:http://www.shlongjin.cn/

Contact:021-56517503,56502257

Address:No.16, Lane 555, Chengyin Road, Shanghai
VanderArk International Limited

Contact:86-10-82437576

Address:Qing He
King Brother Chem Co., Ltd

website:http://www.uvchemkeys.com

Contact:0086-021-58785816

Address:RM2607 Building No.1 Guosheng, Lane 388, Zhongjiang Road, Putuo District, Shanghai 200062 China

Relevant to this article

Doi:10.1021/jo00428a022
(1977)
Design of chiral boronate-substituted acrylanilides. Self-activation and boron-transmitted 1,8-stereoinduction in [4+2] cycloaddition

Doi:10.1016/S0022-328X(03)00400-5
(2003)
11,12 Secoprostaglandins. 3. 8 Alkylthio(sulfinyl and sulfonyl) 12 hydroxyalkanoic acids and related compounds

Doi:10.1021/jm00214a016
(1977)
Electrochemical 1,4-reduction of α,β-unsaturated ketones with methanol and ammonium chloride as hydrogen sources

Doi:10.1039/c9cc02368b
(2019)
(Re)Investigation of the reactivity of uranium hexafluoride toward several organic functions at room temperature

Doi:10.1016/j.jfluchem.2014.06.007
(2014)
A convenient synthesis of papaverine analogs via photocyclization of N-acyl-α-dehydroarylalaninamide derivatives

Doi:10.3987/COM-06-10710
(2006)

Article Doi