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 MoreNanjing HuiBaiShi Biotechnology Co.,Ltd.
Contact:+86 (25)58745219
Address:No.606 Ningliu Road,LiuHe District.
TAIZHOU XINGCHENG CHEMPHARM CO.,LTD.
Contact:0086-0576-88551200,88886292 ,88880039
Address:B Area. 10 Floor.Yaodadasha. 289#.Shifu Road.Taizhou.Zhejiang.China
Shanghai Sunway Pharmaceutical Technology Co.,Ltd.
Contact:+86-21-5161 3915
Address:Shanghai YangPu
Jiangsu Wanlong Chemical Co., Ltd.
website:http://www.wanlongchem.com
Contact:+86-511-86810993 0086-511-8681 0888;
Address:Quanzhou Town, Danyang City, Jiangsu
Zhejiang Kente Chemical Co.,Ltd.
Contact:86-0576-87651912
Address:No.7, Fengxi West Road, Modern Industrial Zone
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)
