Scholarly article on 3-Methyl-3-(4-brom-benzoyl)-acrylsaeure 49661-01-0 from Journal of the American Chemical Society p. 1168,1175

DOI: 10.1021/ja01330a052

Source and publish data:

Journal of the American Chemical Society p. 1168,1175 (1933)

Update date:2022-08-05

Topics:

Authors:

Lutz Lutz

Taylor Taylor

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

Article abstract of DOI:10.1021/ja01330a052

Full text of DOI:10.1021/ja01330a052

Products guided by the article

Product name:3-Methyl-3-(4-brom-benzoyl)-acrylsaeure

Cas No:49661-01-0

R&D Labs maybe for 49661-01-0

Oceachem Group Limited

website:http://www.oceanchem-group.com

Contact:86-536-8596048

Address:9th floor,Building B future Plaza, No.88.Fenghuang Street,Weifang,Shandong,China
Shijiazhuang Frontierchem Co., Ltd.

Contact:+86-311-89271196

Address:4-4-202 No.15 Biandian Street,Shijiazhuang
LianYunGang Chiral Chemical(CHINA) CO.,LTD

Contact:+86-518-83616958 +86-519-82884848

Address:LianYunGang Chemical Industry Park (JiangSu)
zhuzhou zhongle chemical co. ltd.

Contact:+86-0731 28228409

Address:Zhuzhou, Hunan, China
Jinan Hongfangde Pharmatech Co.,Ltd

Contact:86-531-88870908

Address:F Bldg. West Unit North Area of Univ. Tech. Garden Xinyu Rd. Jinan New & High Tech Industry Development Zone Shandong, China

Relevant to this article

Nucleophilic Reactions of F3C^- at sp² and sp³ Carbon in the Gas Phase. Characterization of Carbonyl Addition Adducts

Doi:10.1021/ja00363a010
(1983)
Shifting Chemical Equilibria in Flow - Efficient Decarbonylation Driven by Annular Flow Regimes

Doi:10.1002/anie.201407219
(2014)
Synthesis of highly functionalized phenylalanine derivatives via cross-enyne metathesis reactions

Doi:10.1016/S0040-4020(02)01178-X
(2002)
Doi:10.1039/jr9650007370
(1965)
Antiproliferative activity exerted by tricyclohexylphosphanegold(I) n-mercaptobenzoate against MCF-7 and A2780 cell lines: the role of p53 signaling pathways

Doi:10.1007/s10534-020-00269-7
(2021)
Synthesis of cryptolepine and cryptoteckieine from a common intermediate

Doi:10.1002/1522-2675(200211)85:11<3823::AID-HLCA3823>3.0.CO;2-S
(2002)

Article Doi

DOI: 10.1021/ja01330a052