1-Indancarboxylic Acids. IV. A convenient synthesis of antiinflammatory 4-aroyl-1-indancarboxylic acids and their absolute configurations

DOI: 10.1248/cpb.26.1776

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 1776 - 1785 (1978)

Update date:2022-08-03

Topics:

Authors:

Aono Aono

Kishimoto

Araki Araki

Noguchi Noguchi

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

Article abstract of DOI:10.1248/cpb.26.1776

Full text of DOI:10.1248/cpb.26.1776

NII-Electronic Library Service

Products guided by the article

Product name:4-o-Xyloyl-1-indanon

Cas No:68569-89-1

R&D Labs maybe for 68569-89-1

HENAN NEW BLUE CHEMICAL CO.,LTD

website:http://www.newbluechem.com

Contact:86-371-55170693/55170694

Address:Zhengzhou International Trade New Territory,Jinshui District,Zhengzhou ,China
Arromax Pharmatech Co.,Ltd

website:http://www.arromax.com

Contact:+86-0512-62959601 skype:aimmezhang

Address:Suite 401, Bldg A3, 218 Xinghu St.Suzhou Industrial Park 215123, P.R. China
Shanghai Surseechem Co.,Ltd.

Contact:+86-21-61318535

Address:Building 29,No.2139 Xizha Road, Fengxian District, Shanghai
Hefei Highzone Fine Chemical S&T CO.,LTD

Contact:86-0551-63663560

Address:room 1801 NO. 24 Shuguang RD.
FREEBARQUE DEVELOPMENT GROUP LIMITED

Contact:+86(0)10-5109 5335 or 5109 5345

Address:Room602,Block1-B,LINGDI OFFICE,NO.13 BEIYUAN ROAD

Relevant to this article

Doi:10.1021/jo01321a005
(1979)
Iron(III)picolinate-catalyzed oxygenation of cholesteryl acetate with hydrogen peroxide or peracetic acid

Doi:10.1248/cpb.47.64
(1999)
ON THE PROBLEM OF TWO-ELECTRON REDUCTION OF ARENECYCLOPENTADIENYLIRON CATIONS

Doi:10.1016/S0022-328X(00)86652-8
(1981)
Reduction of alkyl halides by triethylsilane based on a cationic iridium bis(phosphinite) pincer catalyst: Scope, selectivity and mechanism

Doi:10.1002/adsc.200800528
(2009)
Synthesis of diastereoisomeric 4-dimethylamino-3-phenyl-2-butanols and related esters for antimicrobial evaluation

Doi:10.1002/jps.2600670335
(1978)
CD4 mimics as HIV entry inhibitors: Lead optimization studies of the aromatic substituents

Doi:10.1016/j.bmc.2013.02.041
(2013)

Article Doi