Scholarly article on 2-[2-(3,3-dimethyl-1-oxo-1,3-dihydro-1λ5-benzo[c][1,2]oxaphosphol-1-yl)-phenyl]-propan-2-ol 67771-45-3 from Journal of the American Chemical Society p. 5229 - 5230

DOI: 10.1021/ja00484a064

Source and publish data:

Journal of the American Chemical Society p. 5229 - 5230 (1978)

Update date:2022-08-06

Topics:

Authors:

Granoth,I.

Martin,J.C.

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

Article abstract of DOI:10.1021/ja00484a064

Full text of DOI:10.1021/ja00484a064

Products guided by the article

Product name:2-[2-(3,3-dimethyl-1-oxo-1,3-dihydro-1λ⁵-benzo[c][1,2]oxaphosphol-1-yl)-phenyl]-propan-2-ol

Cas No:67771-45-3

R&D Labs maybe for 67771-45-3

JADECHEM NINGBO CO.,LTD.

Contact:+86-574-89075960

Address:#100 Xiang Yun Road, New High tech area, Ningbo, China
Shanghai UCHEM Inc.

Contact:+86-21-56338808

Address:799 Dunhuang Road, Putuo
Nanjing Chemipioneer Pharma&Tech Co.,Ltd

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

Contact:+86-25-52685700

Address:Room 305，A Block，Biological-Medicine Building，Business Start-up Center，Xin-ke 1st Road, High-tech development zone，Nanjing city，Jiangsu Province, China
DU-HOPE INTERNATIONAL GROUP

Contact:+86-25-52346955

Address:199,JIANYE ROAD,NANJING,CHINA
sichuan tiancai fine co LTD.

website:http://www.tcfinechem.com/

Contact:18681346930

Address:baifu town,whou district

Relevant to this article

Doi:10.1021/jo00419a046
(1978)
Doi:10.1021/jf60220a006
(1978)
Biphasic glycerol/2-MeTHF, ruthenium-catalysed enantioselective transfer hydrogenation of ketones using sodium hypophosphite as hydrogen donor

Doi:10.1002/ejoc.201300506
(2013)
An efficient regioselective three-component synthesis of tetrazoloquinazolines using g-C3N4 covalently bonded sulfamic acid

Doi:10.1016/j.poly.2019.114217
(2020)
Davis-Beirut reaction: Route to thiazolo-, thiazino-, and thiazepino-2 h -indazoles

Doi:10.1021/jo501014e
(2014)
Design, synthesis, and structure-activity relationship studies of N-arylsulfonyl morpholines as γ-secretase inhibitors

Doi:10.1016/j.bmcl.2010.09.028
(2010)

Article Doi

DOI: 10.1021/ja00484a064