Scholarly article on [phenyl-(2-phenyl-1,3-dioxolan-2-yl)methyl] acetate 6963-16-2 from Journal of the American Chemical Society p. 633,637

DOI: 10.1021/ja01512a032

Source and publish data:

Journal of the American Chemical Society p. 633,637 (1959)

Update date:2022-08-04

Topics:

Authors:

Summerbell

Berger Berger

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

Article abstract of DOI:10.1021/ja01512a032

Full text of DOI:10.1021/ja01512a032

Products guided by the article

Product name:[phenyl-(2-phenyl-1,3-dioxolan-2-yl)methyl] acetate

Cas No:6963-16-2

R&D Labs maybe for 6963-16-2

Jiangsu Taihu New Materials Holding Co., Ltd

Contact:+86-519-86160108

Address:Xueyan Town, Changzhou City, Jiangsu Province, 213169, China
Shanghai Standard Biotech Co., Ltd.

Contact:+86-18502101150

Address:Room 103, Building 2nd, NO.720, Cailun Road , Pudong District, Shanghai, China
Foreschem Co., Ltd

Contact:+86-533-3112891

Address:zibo
Zhejiang Allied Chemical Co.,Ltd

Contact:18967038207

Address:Area A-30, High-tech Industrial Park, Quzhou, Zhejiang, China.
FREEBARQUE DEVELOPMENT GROUP LIMITED

Contact:+86(0)10-5109 5335 or 5109 5345

Address:Room602,Block1-B,LINGDI OFFICE,NO.13 BEIYUAN ROAD

Relevant to this article

Palladium-Catalyzed Umpolung Type-II Cyclization of Allylic Carbonate-Aldehydes Leading to 3-Methylenecycloalkanol Derivatives

Doi:10.1002/adsc.201900450
(2019)
2,2,3-TRIARYLPROPIONITRILES AND RELATED COMPOUNDS AS

Doi:10.1021/jm00341a014
(1963)
Cyclocondensation reaction of 4-aryl-4-methoxy-1,1,1-trifluoro-3-buten-2-ones with urea Synthesis of novel 6-aryl(5-methyl)-4-trifluoromethyl-2(1H)-pyrimidinones

Doi:10.1016/S0022-1139(02)00287-7
(2003)
Synthesis and biological evaluation of 3'-carboranyl thymidine analogues.

Doi:10.1016/S0960-894X(02)00357-8
(2002)
Synthesis and activity of new aryl- and heteroaryl-substituted pyrazole inhibitors of the transforming growth factor-β type I receptor kinase domain

Doi:10.1021/jm0205705
(2003)
Doi:10.1021/ja01227a032
(1945)

Article Doi

DOI: 10.1021/ja01512a032