109057-73-0Relevant articles and documents
A mild, selective method for preparation of vicinal fluoro ethers using 'F-Teda-BF4
Stavber,Sotler,Zupan
, p. 1105 - 1108 (1994)
Vicinal alkoxy fluorides are efficiently formed by room temperature reaction of phenyl substituted alkenes with commercially available 1- chloromethyl-4-fluoro-1,4-diazobicyclo[2.2.2]octane bis tetrafluoroborate (Selectfluor(TM) F-Teda BF4) in
FLUORINATION WITH CAESIUM FLUOROXYSULPHATE. ROOM TEMPERATURE FLUORINATION OF PHENYL SUBSTITUTED OLEFINS
Stavber, Stojan,Zupan, Marko
, p. 5035 - 5044 (2007/10/02)
Room -temperature fluorination of 1,1-diphenylethene with caesium fluoroxysulphate in methylene chloride resulted in an addition elimination process, thus yielding 1,1-diphenyl-2-fluoroethene, while in the presence of nucleophile containing species, i.e.,