Scholarly article on 1-{2-[4-(acetyloxy)-3-methoxyphenyl]-2-oxoethyl}pyridinium 6278-20-2 from Journal of the American Chemical Society p. 1913,1916

DOI: 10.1021/ja01214a013

Source and publish data:

Journal of the American Chemical Society p. 1913,1916 (1946)

Update date:2022-08-04

Topics:

Authors:

Riegel Riegel

Wittcoff

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

Article abstract of DOI:10.1021/ja01214a013

Full text of DOI:10.1021/ja01214a013

Products guided by the article

Product name:1-{2-[4-(acetyloxy)-3-methoxyphenyl]-2-oxoethyl}pyridinium

Cas No:6278-20-2

R&D Labs maybe for 6278-20-2

HANWAYS CHEMPHARM CO.,LIMITED

website:http://www.hanwayschem.com

Contact:+86-18502787239(whatsapp)-

Address:18-1-802, Green Garden, Jianghan District, Wuhan 430023, China
Beijing ZhongDaXinHe Chemical Product Co.,Ltd(expird)

Contact:010-52876516

Address:tongzhoubeiyuan
Shenyang Xingzhenghe Chemical Co., Ltd.

Contact:024-23509232

Address:No. 33, Naner Road, Heping Dist.
Oren Hydrocarbons (Qingdao) Co., Ltd.

Contact:+86-532-68607667-801

Address:Room 3 # 302, No.9 Qingyun Road, Qingdao, China
Shangyu Sanhechemicals Co.,LTD.

Contact:86-0571-56696839

Address:Num.2952,Nanhuan Road,Binjiang District,Hangzhou,China

Relevant to this article

Synthesis of the tris-cyclometalated complex fac-[Rh(ptpy)₃] and X-ray crystal structure of [Rh(acac)(ptpy)₂]

Doi:10.1016/j.inoche.2010.12.005
(2011)
Synthesis of novel thioethers and sulfoxide compounds

Doi:10.1080/10426507.2012.757610
(2013)
Doi:10.1139/v63-140
(1963)
Nickel-Catalyzed Aminoxylation of Inert Aliphatic C(sp³)-H Bonds with Stable Nitroxyl Radicals under Air: One-Pot Route to α-Formyl Acid Derivatives

Doi:10.1021/acs.orglett.7b00479
(2017)
A general strategy to Aspidosperma alkaloids: Efficient, stereocontrolled synthesis of tabersonine [6]

Doi:10.1021/ja983198k
(1998)
Generation of o-quinone α-carbomethoxymethide by photolysis of methyl 2-hydroxyphenyldiazoacetate in aqueous solution

Doi:10.1039/b211444p
(2003)

Article Doi

DOI: 10.1021/ja01214a013