An alternate synthesis of 2 (4 isobutylphenyl) propionic acid

DOI: 10.1271/bbb1961.40.291

Source and publish data:

Agricultural and Biological Chemistry p. 291 - 295 (1976)

Update date:2022-08-04

Topics:

Authors:

Kogure Kogure

Nakagawa

Fukawa Fukawa

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

Article abstract of DOI:10.1271/bbb1961.40.291

Full text of DOI:10.1271/bbb1961.40.291

Products guided by the article

Product name:2-Hydroxy-3-(4-isobutyl-phenyl)-but-3-enoic acid

Cas No:53500-85-9

R&D Labs maybe for 53500-85-9

Shandong Dayi Chemical Co., Ltd.

website:http://www.dayi.com.cn

Contact:+86- 535-7388728. 15306386031

Address:No 1 Danya west road, Laiyang City, Shandong province
Jiangsu Haian Petro chemical Plant

Contact:+86-513-88902723

Address:99, Changjiang West Road, Haian County, Jiangsu
Du-Hope International Group

website:http://www.np-chem.com

Contact:0086-25-52346877

Address:199, Jian Ye Road, Nanjing, China
JinTan Pingsheng Chemical Co.,Ltd

Contact:+86-519-82828200

Address:NO.11Danfengxilu Road,Jintan City,Jiangsu,China
WD Silicone Co., Ltd

Contact:+86-27-87204219, +86-27-87215023

Address:2402, HuiGu Space-time Building, 8 Forest Road, East Lake Hi-Tech Development Zone

Relevant to this article

A Facile and General, One-pot Synthesis of 2-Oxoalkane Phosphonates from Diethylphosphonocarboxylic Acid Chlorides and Organometallic Reagents

Doi:10.1055/s-1986-31739
(1986)
Novel alternative for the N-N bond formation through a PIFA-mediated oxidative cyclization and its application to the synthesis of indazol-3-ones

Doi:10.1021/jo060070+
(2006)
Pyridine-containing nickel(II) bis-formazanates: Synthesis, structure, and electrochemical study

Doi:10.1007/s11172-006-0491-9
(2006)
Yonemitsu-type condensations catalysed by proline and Eu(OTf)₃

Doi:10.1039/c4ra08853k
(2014)
Metal-Free Synthesis of α-Aminophosphonates from Tertiary Amines and P(O)H Compounds via a Cross-Dehydrogenative Coupling Reaction

Doi:10.1055/s-0037-1610306
(2018)
Ruthenium cryptates with an unusual selectivity for nitrate

Doi:10.1039/c2dt12446g
(2012)

Article Doi