Scholarly article on (3,4,5-triacetoxy-phenyl)-acetic acid methyl ester 100976-93-0 from Journal of the American Chemical Society p. 179,184

DOI: 10.1021/ja01558a049

Source and publish data:

Journal of the American Chemical Society p. 179,184 (1957)

Update date:2022-07-30

Topics:

Authors:

Goodwin Goodwin

Witkop Witkop

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

Article abstract of DOI:10.1021/ja01558a049

Full text of DOI:10.1021/ja01558a049

Products guided by the article

Product name:(3,4,5-triacetoxy-phenyl)-acetic acid methyl ester

Cas No:100976-93-0

R&D Labs maybe for 100976-93-0

MTT Pharma & Bio-technology Co.,Ltd(expird)

Contact:+86-21-58407925

Address:Room2019, Building C, Tomson Center, No.158, Zhang Yang Road, Shanghai, China
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
VanderArk International Limited

Contact:86-10-82437576

Address:Qing He
Shanghai united Scientific Co.,Ltd.

Contact:+86-21-53535353

Address:28F No.900 huaihai Road Shanghai China
zhenjiang runjing high purity chemical co ltd

Contact:+86-511-83361155

Address:No.8.haixi road,international chemical park

Relevant to this article

Design, synthesis, evaluation, and crystallographic-based structural studies of HIV-1 protease inhibitors with reduced response to the V82A mutation

Doi:10.1021/jm701170f
(2008)
Gold-catalyzed intermolecular hetero-dehydro-Diels-Alder cycloaddition of captodative dienynes with nitriles: A new reaction and regioselective direct access to pyridines

Doi:10.1021/ja7112917
(2008)
Alkylation of Sulfonamides with Trichloroacetimidates under Thermal Conditions

Doi:10.1021/acs.joc.6b01421
(2016)
Importance of the hydroxymethyl - Quinuclidine fragment in the catalytic asymmetric aldol reactions utilizing quaternary ammonium fluorides derived from cinchona alkaloids

Doi:10.3987/COM-95-S28
(1996)
Metal-free catalytic synthesis of diaryl thioethers under mild conditions

Doi:10.1039/c6nj00322b
(2016)
Pre-activation protocol leading to highly stereoselectivity-controllable glycosylations of oxazolidinone protected glucosamines

Doi:10.1039/b712591g
(2008)

Article Doi

DOI: 10.1021/ja01558a049