Journal of the Chemical Society. Perkin transactions I p. 553 - 557 (1989)
Update date:2022-09-26
Topics:
Barluenga, Jose
Foubelo, Francisco
Fananas, Francisco J.
Yus, Miguel
N-Phenyl or N-benzoyl 2-halogenoallylamines (5) or (10) react successively with phenyl-lithium and lithium naphthalenide at -78 deg C to give the intermediates (4) or (11), which on reaction with electrophiles (water, deuterium oxide, dimethyl disulphide, aldehydes, ketones, or allyl bromide) yield functionalized allyl amines (6) and (12).The corresponding N-alkyl derivatives (9) afford prop-2-ynylamines (8) under the same reaction conditions.
View MoreContact:86-513-84128750/13773795976
Address:No.48.Youyi West Road ,Rudong Development Zone,Jiangsu Province,China
Shandong Topscience Biotech Co., Ltd.
Contact:0633-2619278
Address:No. 98 Lanshan West Road, Lanshan District, Rizhao, Shandong Province, P.R. of China
Shanghai Hohance Chemical Co., ltd
Contact:13914753421
Address:Fl.5；Bld. 70, Lane 1500; Xinfei Road
Nanjing Ruizhi Industry & Technologh Co.，Ltd.
Contact:+86-25-86808110
Address:441-4-A5,NO.12 Longzang Avenue,Yuhuatai District,210039,Nanjing
Contact:0311-13263231263
Address:jian hua street,Shijiazhuang City, China
Doi:10.1007/BF00519828
(1985)Doi:10.1002/chem.200700832
(2007)Doi:10.1021/jo701944c
(2008)Doi:10.1021/jm00150a002
(1985)Doi:10.1002/ejoc.201101784
(2012)Doi:10.1080/00397910903162775
(2010)
