Journal of Fluorine Chemistry p. 231 - 236 (1986)
Update date:2022-08-03
Topics: Regioselectivity Column chromatography Yield NMR spectroscopy Mass spectrometry nucleophiles TLC (thin-layer chromatography) Anhydrous conditions Oxidative Addition Reductive Elimination Reaction Mechanism Solvent Effects Stereoselectivity Catalysis Perfluoroalkyl Groups Hypervalent Iodine Compounds Triflates Electrophilic fluorination
Umemoto, Teruo
Gotoh, Yoshihiko
It was demonstrated that (1,1-dihydroperfluoroalkyl)phenyliodonium triflates (FMITS) served as very useful sources of 1,1- dihydroperfluoroalkyl cations. With a variety of nucleophiles, the corresponding fluoroalkyl derivatives were obtained.
View MoreChengdu King-tiger Pharm-chem. Tech. Co., Ltd
Contact:028-85317716
Address:Tianfu Life Science Park, No. 88 South Keyuan Road, Gaoxin District, Chengdu City, Sichuan Province, PRC.
Nanjing distinctions Medical Technology Co., Ltd.(expird)
Contact:+86-15996203785 13914714059
Address:nanjing,jiangsu , China
Shaanxi Sinuote Biotech Co.,Ltd
Contact:+86-29-68859685
Address:No 18,Taiyuan Road ,Xi'an city ,China
lianyungang jinkang pharmaceutical technology co., ltd.
Contact:008651885445517
Address:Jinshan industrial park, Ganyu county, Lianyungang, Jiangsu Province, 222115, China
Taizhou Chenyi chemical co. LTD,
Contact:13736652831
Address:NO.273 SHANGHAI SOUTH STREET,LUQIAO DISTRICT,ZHEJIANG PROVINCE,CHINA.
Doi:10.1039/d0gc04395h
(2021)Doi:10.1021/acs.orglett.8b02840
(2018)Doi:10.1021/ol0066375
(2000)Doi:10.1016/j.parint.2017.03.006
(2017)Doi:10.1016/S0957-4166(00)82289-2
(1992)Doi:10.1016/S1387-7003(03)00014-5
(2003)
