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

YORK CHEMICALS LTD

Contact:+1 (647) 918 5848

Address:2343 BRIMLEY RD., Suite 250
Guangzhou Swan Chemical Co., Ltd.

Contact:+86-20-31075659

Address:NO.301, Hong ba fang investment BLDG 1,Guan chong village,Shiqi town,Panyu district,Guangzhou
Anhui New Star Pharmaceutical Development Co., Ltd

Contact:013956922763

Address:Floor 3, F9A, F Workshop, No.110 Kexue Road, High-Tech Development Zone, Hefei, Anhui ,China
Shanghai Dianyang Industry Co.,ltd

Contact:+86 21 6492 4669

Address:Chejing RD, Songjiang District, Shanghai, China
Chongqing maohuan Chemicals Co., Ltd

website:http://www.bschem.com

Contact:+86 13996103726

Address:Chongqing Nan'an District Tu Town

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