An improved method for the preparation of 3-substituted 10,11-dihydro-5H-[b,f] azepine derivatives

DOI: 10.1002/prac.199733901104

Source and publish data:

Advanced Synthesis and Catalysis p. 587 - 589 (1997)

Update date:2022-08-25

Topics:

Authors:

Csende, Ferenc

Hosztafi, Sándor

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

Article abstract of DOI:10.1002/prac.199733901104

Full text of DOI:10.1002/prac.199733901104

Products guided by the article

Product name:5-ACETYLIMINODIBENZYL 99

Cas No:13080-75-6

R&D Labs maybe for 13080-75-6

Shandong Jincheng Zhonghua Bio-pharmaceutical Co.,Ltd

Contact:+86-533-5415882

Address:Zichuan Economic Development Zone,Zibo City,Shandong Province,China
Hangzhou Maytime Bio-Tech Co.,Ltd.

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

Contact:+86-571-88925295 88920965

Address:NO.2-1701 Ganghui Central Ningwei Street, Xiaoshan Hangzhou Zhejiang China
Jiangsu Cale New Material Co.ltd

Contact:+86-515-88334667/88203550

Address:Zhongshan 3rd Road, Coastal Chemical Industry Park, Yancheng, Jiangsu, China
Hangzhou Share Chemical Co., Ltd(expird)

Contact:+86-57187093700

Address:Hang Xing Road
Beijing ZhongDaXinHe Chemical Product Co.,Ltd(expird)

Contact:010-52876516

Address:tongzhoubeiyuan

Relevant to this article

Doi:10.1039/c29690000871
(1969)
Hydrothermal synthesis, structure, heterogeneous catalytic activity and photoluminescent properties of a novel homoleptic Sm(III)-organic framework

Doi:10.1016/j.jssc.2016.09.018
(2016)
Cross-metathesis of vinylsilanes with olefins in the presence of Grubbs' catalyst

Doi:10.1016/S0040-4039(00)02201-2
(2001)
Enantioselective Catalytic Isomerization of an Unfunctionalized Achiral Alkene

Doi:10.1021/ja00032a062
(1992)
Enantiopure (S)-4-phenyl-3-butyn-2-ol and (S)-1-phenyl-2-butanol through an enzymatic reduction

Doi:10.14233/ajchem.2014.17456
(2014)
Synthesis, structural, spectroscopic, and thermal studies of some transition-metal complexes of a ligand containing the amino mercapto triazole moiety

Doi:10.1002/aoc.5591
(2020)

Article Doi