Journal of Fluorine Chemistry p. 67 - 86 (1989)
Update date:2022-07-30
Topics:
Ono, Taizo
Inoue, Yoshihisa
Arakawa, Yoshio
Naito, Youichiro
Fukaya, Chikara
Electrochemical fluorination of N-cyclopentylpyrrolidine gave the corresponding F-amine together with a ring-opened compound N-(F-pentyl)-F-pyrrolidine in the ratio of 1 to 1, in 55 percent yield.N-cyclohexylpyrrolidine, N-cyclopentylpiperidine and N-cyclohexylpiperidine were also electrochemically fluorinated in the same manner to give the corresponding F-amines, their isomers with rearranged structures, and ring-opened ones, in the ratio of ca. 4:2:1, 2:1:1, and 2:1:1, respectively in 51 to 53 percent yields.Supporting spectral data are presented.
View MoreContact:86-511-85210668 0511-85210668, 85210818, 85210898
Address:Yihai Garden E-902,NO.99 Daxi RD., Zhenjiang Jiiangsu ,China
Contact:86-898-65311214
Address:Room 102, BLDG. 68 Jiangnan City, No. 66 Heping Road,Haikou, Hainan, China
Shandong Bolode Bio-Technology Co., LTD
Contact:+86-0531-58966870
Address:136 Jingyi Road,Huaiyin District,Jinan,Shandong,China
Contact:0571-
Address:zhejing
Geen Chemical Technology Co., Ltd
Contact:86-769-21660847
Address:1408, Yingfeng Commercial Center, Nancheng District
Doi:10.1021/jacs.7b07658
(2017)Doi:10.1021/jo048172s
(2005)Doi:10.1002/jhet.5570430205
(2006)Doi:10.1016/j.ica.2004.11.031
(2005)Doi:10.1021/jm0492498
(2005)Doi:10.1016/0040-4020(82)85160-0
(1982)