Journal of the American Chemical Society p. 2497 - 2501 (1982)
Update date:2022-08-03
Topics: Oxidation Cyclization Product Formation Nucleophilic Attack Carbonyl Compounds Trivalent Phosphorus Compounds Oxidants
Harper, S. D.
Arguengo, Anthony J.
Phosphonous diesters derived from the reaction of phenylphosphonous dichloride with 2-ketophenols readily undergo head-to-tail intramolecular cyclization in cases where the carbonyl function is an aldehyde, trifluoromethylacetophenone, or diaryl ketone.A
View Morewebsite:http://www.greenutra.cn
Contact:0086-411-39553357
Address:No. 7-1-1802, Huizhi Garden,Ocean Square,Dalian, 116033, China
Nanjing HuiBaiShi Biotechnology Co.,Ltd.
Contact:+86 (25)58745219
Address:No.606 Ningliu Road,LiuHe District.
Contact:+86-(0)21-3770 9035
Address:Room 301, Building 2, Meijiabang Road 1508, Shanghai China
Taizhou Crene Biotechnology co.ltd
Contact:86-576-88813233 88205808
Address:Economic Developed Zone of Taizhou Zhejiang China
Shanghai Yurui Biotechnology(Anyang) Pharmaceutical Co., Ltd
Contact:+86-0372-3662335 +86-0372-3661988
Address:hanling industrial park anyang
Doi:10.1055/s-1982-29760
(1982)Doi:10.1016/j.poly.2016.06.047
(2016)Doi:10.1016/j.bcp.2004.02.011
(2004)Doi:10.1002/ardp.19823150910
(1982)Doi:10.1021/acs.jmedchem.6b01033
(2016)Doi:10.1016/j.bmcl.2008.11.030
(2009)
