Scholarly article on 3-benzyl-2-oxo-3,4-diphenyl-butyric acid 102591-91-3 from Bulletin of the Chemical Society of Japan p. 351,354

DOI: 10.1246/bcsj.31.351

Source and publish data:

Bulletin of the Chemical Society of Japan p. 351,354 (1958)

Update date:2022-08-05

Topics:

Authors:

Ando Ando

Tokura Tokura

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

Article abstract of DOI:10.1246/bcsj.31.351

Full text of DOI:10.1246/bcsj.31.351

Products guided by the article

Product name:3-benzyl-2-oxo-3,4-diphenyl-butyric acid

Cas No:102591-91-3

R&D Labs maybe for 102591-91-3

NingBO Hong Xiang Biochem.Co.Ltd

website:http://www.hxbiochem.com

Contact:0574-66003444

Address:Ning Bo Bei Lun
JIANGSU GRAND XINYI PHARMACEUTICAL CO.,LTD

website:http://www.xypharm.com/

Contact:+86-515-84383317

Address:Chenli Road,Costal Chemical Area Binhai,Yancheng, Jiangsu,China
Jinzhou Jiutai Pharmaceutical Co.,Ltd

Contact:+86-0416-5179890

Address:No.41, Taianli, Taihe District, Jinzhou, Liaoning
Shijiazhuang Frontierchem Co., Ltd.

Contact:+86-311-89271196

Address:4-4-202 No.15 Biandian Street,Shijiazhuang
Chengdu Pukang Biotechnology Co., Ltd

website:http://www.pu-kang.com

Contact:86-028-63976226

Address:No. 868 Xiwang Road,Xinjin county,Chengdu city, China

Relevant to this article

1-arylnaphthalene lignan: A novel scaffold for type 5 phosphodiesterase inhibitor

Doi:10.1021/jm9807048
(1999)
The Stereoselective Synthesis of Acyclic and Exocyclic Trisubstituted Olefins via a Hydroxyl-Directed Wittig Reaction

Doi:10.1021/jo00388a063
(1987)
Control of the photoreactivity of diarylethene derivatives by quaternarization of the pyridylethynyl group

Doi:10.1021/ol8005216
(2008)
Enzyme-catalysed Synthesis of Peptides containing D-Amino Acids

Doi:10.1039/c39860000417
(1986)
Indanesulfonamides as carbonic anhydrase inhibitors. Toward structure-based design of selective inhibitors of the tumor-associated isozyme CA IX

Doi:10.1021/jm0600287
(2006)
Visible-Light-Induced Nickel-Catalyzed Cross-Coupling with Alkylzirconocenes from Unactivated Alkenes

Doi:10.1016/j.chempr.2019.12.010
(2020)

Article Doi

DOI: 10.1246/bcsj.31.351