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 MoreMTT Pharma & Bio-technology Co.,Ltd(expird)
Contact:+86-21-58407925
Address:Room2019, Building C, Tomson Center, No.158, Zhang Yang Road, Shanghai, China
wuxi huabin bio-tech Co.,Ltd(expird)
Contact:86-0510-85133006
Address:hubin road NO157
Contact:+86-574- 87178138; 87297407
Address:No. 809, Liudingxingzuo, cangsong road, Ningbo, China
Hangzhou J&H Chemical Co., Ltd.
website:http://www.jhechem.com/
Contact:+86-571-87396432
Address:No.200 Zhenhua Rd.Xihu Industrial Park, Hangzhou 310030, China
shijiazhuang baisheng chem co.; ltd
Contact:86-0311-80790826
Address:shijiazhuang hebei
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)
