Journal of the Chemical Society. Chemical communications p. 242 - 244 (1986)
Update date:2022-07-29
Topics:
Tanaka, Jiro
Nojima, Masatomo
Kusabayashi, Shigekazu
The reaction of 1-arylpropenyl-lithium (1a-c) with t-alkyl bromides proceeds by either a nucleophilic substitution or single electron transfer mechanism, the preferred pathway being a function of electronic substituent effects and the absence or presence of tetramethylethylenediamine or hexamethylphosphoramide.
View MoreHubei Onward Bio-Development Co., Ltd.
Contact:+86-718-8417012
Address:No.517,Shizhou Avenue,Enshi City,Hubei Province,China,445002
Contact:86 513 85512619
Address:Rm.1306, Building A, Wenfeng Mansion,168 Gongnong Road, Nantong Jiangsu China
Tangshan Moneide Trading Co., Ltd.
Contact:+86-315-8309571
Address:2-7-420 Jidong Building Materials Commercial Center, Tangshan, Hebei, 064000 China
Changzhou Anyi Biochem Co., Ltd.(expird)
Contact:+86-519-88836158
Address:no,51 caoda
Shandong Ailitong New Material Co.,Ltd
Contact:+86-536-3226266
Address:zhongjia village, putong town , qingzhou city,Shandong Province,China
Doi:10.1055/s-2008-1077962
(2008)Doi:10.1016/0039-128X(86)90076-0
(1986)Doi:10.1016/S0040-4020(01)90616-7
(1986)Doi:10.1016/j.molcata.2014.09.040
(2015)Doi:10.1021/jm00387a014
(1987)Doi:10.1021/ic8006475
(2008)
