Non-steroidal antiinflammatory agents. 3. [1]. Synthesis of 3-hydroxy-3-hydroxyphenyl-2,4-dioxo-1,2,3,4-tetrahydroquinolines

DOI: 10.1002/jhet.5570220431

Source and publish data:

Journal of Heterocyclic Chemistry p. 1081 - 1087 (1985)

Update date:2022-08-05

Topics:

Authors:

Faber Faber

Steininger

Kappe Kappe

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

Article abstract of DOI:10.1002/jhet.5570220431

Full text of DOI:10.1002/jhet.5570220431

Products guided by the article

Product name:3-hydroxy-3-(4-hydroxy-3-methylphenyl)-1-methyl-2,4-dioxo-1,2,3,4-tetrahydroquinoline

Cas No:102249-38-7

R&D Labs maybe for 102249-38-7

FOSHAN NANHAI ZHONGNAN PHARMACEUTICAL FACTORY

Contact:0086-0757-85609331

Address:XIAHENGTIAN INDUSTRIAL ZONE,SHAYONG VILLAGE,LISHUI TOWN
GUANGZHOU MEDCAN PHARMATECH LTD

website:http://www.gzmedcan.com

Contact:+86-20-82519649

Address:Building J,Room 101,1 JiangtashanRd,Guang Zhou Science City,Guang Zhou ,China
Luoyang Aoda chemical Co.,Ltd.

Contact:+86-379-67518785 67516588

Address:MiaoWan industry district,YanShi City,Henan,China
Hotechem Shanghai Co., Ltd

Contact:13120882795；+86-21-34621078;+86-021-31122318

Address:Suite 2,No.2715 Longwu Road
Jiangsu Haian Petro chemical Plant

Contact:+86-513-88902723

Address:99, Changjiang West Road, Haian County, Jiangsu

Relevant to this article

Promotion of sugar-lectin recognition through the multiple sugar presentation offered by regioselectively addressable functionalized templates (RAFT): A QCM-D and SPR study

Doi:10.1039/b716214f
(2008)
Bacterial transferase MraY inhibitors: Synthesis and biological evaluation

Doi:10.1016/j.bmc.2010.04.023
(2010)
Novel uracil-based 2-aminoanilide and 2-aminoanilide-like derivatives: Histone deacetylase inhibition and in-cell activities

Doi:10.1016/j.bmcl.2008.03.055
(2008)
Concise enantioselective synthesis of (+)-FR66979 and (+)-FR900482: Dimethyldioxirane-mediated construction of the hydroxylamine hemiketal

Doi:10.1002/anie.200290015
(2002)
Synthesis, characterization of novel cyclohexenone derivatives and computation of their optical response

Doi:10.1016/j.molstruc.2014.04.074
(2014)
Doi:10.1021/jo01095a024
(1958)

Article Doi