Scholarly article on 2-[(R)-1-methoxy-2-(4-nitro-benzoyloxy)-ethoxy]-1,3-bis-(4-nitro-benzoyloxy)-propane 10563-74-3 from Journal of the American Chemical Society p. 3091,3093, 3095

DOI: 10.1021/ja01616a047

Source and publish data:

Journal of the American Chemical Society p. 3091,3093, 3095 (1955)

Update date:2022-07-29

Topics:

Authors:

Smith Smith

Van Cleve

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

Article abstract of DOI:10.1021/ja01616a047

Full text of DOI:10.1021/ja01616a047

Products guided by the article

Product name:2-[(R)-1-methoxy-2-(4-nitro-benzoyloxy)-ethoxy]-1,3-bis-(4-nitro-benzoyloxy)-propane

Cas No:10563-74-3

R&D Labs maybe for 10563-74-3

Taixing Joxin Bio-tec Co.,Ltd.

website:http://www.joxbio.com

Contact:86-523-87558858 87612088

Address:No.88, chengdong industrial park
ZHEJIANG JIANYE CHEMICAL CO.,LTD.

Contact:86-571-64149273,64149234

Address:No. 48, Fuxi Road, Meicheng Town
Advanced Biotech

Contact:+1-973-357-0577

Address:10 Taft Rd.
puyang hongda shengdao new material co.,ltd.

Contact:+86-393- 4896278

Address:No.29 East Zhongyuan Road
KA-SHING Business Trade Macau Co., Ltd.

Contact:00853-28430045

Address:23rd Floor, Block 3 La Cite, Areia Preta, Macao

Relevant to this article

Targeting the human parasite Leishmania donovani: Discovery of a new promising anti-infectious pharmacophore in 3-nitroimidazo[1,2-a]pyridine series

Doi:10.1016/j.bmc.2013.09.002
(2013)
Doi:10.1021/ja01575a053
(1957)
Hydrogen bonding and Lewis acid-base interactions in the system bis(pentafluorophenyl)borinic acid/methanol

Doi:10.1002/ejic.200701210
(2008)
Regioselective cobalt-catalyzed Diels-Alder reaction towards 1,3-disubstituted and 1,2,3-trisubstituted benzene derivatives

Doi:10.1055/s-2008-1078450
(2008)
ASYMMETRIC BROMOLACTONIZATION REACTION: SYNTHESIS OF OPTICALLY ACTIVE 2-HYDROXY-2-METHYLALKANOIC ACIDS FROM 2-METHYLENEALKANOIC ACIDS

Doi:10.1016/S0040-4039(00)96213-0
(1987)
FACILE SYNTHESIS OF 2-METHYLENE-4-BUTYROLACTONES

Doi:10.1246/cl.1986.541
(1986)

Article Doi

DOI: 10.1021/ja01616a047