Ring closure of 1-[4-(Imidazol-1-yl)phenyl]-3-phenyl-2-propen-1-one derivatives to potential biologically active compounds

DOI: 10.1002/jhet.5570300444

Source and publish data:

Journal of Heterocyclic Chemistry p. 1093 - 1095 (1993)

Update date:2022-07-29

Topics:

Authors:

Coudert Coudert

Couquelet

Tronche Tronche

Leal Leal

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

Article abstract of DOI:10.1002/jhet.5570300444

Full text of DOI:10.1002/jhet.5570300444

Products guided by the article

Product name:2-cyano-3-phenyl-5-oxo-5-<4-(imidazoyl-1-yl)phenyl>pentanamide

Cas No:154012-92-7

R&D Labs maybe for 154012-92-7

Wuxi Olite Chemical Co., Ltd.

Contact:86-510-82853889

Address:Rm.3732, No.18-2,Yonghe Rd.,Wuxi,Jiangsu,214023,China
Zhuhai Rundu Pharmaceutical co.,Ltd

Contact:+86-756-7630755

Address:No.6,North Airport Road,Sanzao Town,Jinwan District
Beijing ZhongDaXinHe Chemical Product Co.,Ltd(expird)

Contact:010-52876516

Address:tongzhoubeiyuan
Beijing Zhongshuo Pharmaceutical T & D Co.,Ltd

Contact:0086-10-64430626

Address:ea No 16, HEPINGLI,DONGCHENG DISTRICT,BEIJING,P.R.CHINA.
Hangzhou jls Flame Retardants Chemical Co.,Ltd

Contact:+86-571-87250387/87250386

Address:MOGANSHAN RODA 1418# SHANGCHENG INDUSTRIAL PARK

Relevant to this article

Reaction of 6-Oxa-3-silabicyclo<3.1.0>hexanes with Phosphinimines. Synthesis of 6-Vinyl-1,3-dioxa-2,4-disilacyclohexanes

Doi:10.1246/cl.1987.237
(1987)
Total synthesis, assignment of the absolute stereochemistry, and structure-activity relationship studies of subglutinols A and B

Doi:10.1002/asia.201000147
(2010)
Synthesis of 3-aminoisoxazoles via the addition-elimination of amines on 3-bromoisoxazolines

Doi:10.1021/ol9000284
(2009)
Cobalt-catalyzed aerobic oxidation of (E)- and (Z)-bishomoallylic alcohols

Doi:10.1016/j.tetlet.2008.12.040
(2009)
Trisulfur Radical Anion (S₃^?-) Involved [1 + 2 + 2] and [1 + 3 + 1] Cycloaddition with Aromatic Alkynes: Synthesis of Tetraphenylthiophene and 2-Benzylidenetetrahydrothiophene Derivatives

Doi:10.1021/acs.orglett.8b02066
(2018)
Doi:10.1139/v57-083
(1957)

Article Doi