157928-46-6Relevant articles and documents
Synthesis of sulfanylated difluoroalkenes: Electrophilic difluoromethylidenation of dithioesters with difluorocarbene
Takayama, Ryo,Yamada, Atsushi,Fuchibe, Kohei,Ichikawa, Junji
, p. 5050 - 5053 (2017)
Electrophilic difluoromethylidenation of dithioesters was achieved in high yields via the reaction with difluorocarbene. When aryl or alkyl dithiocarboxylates were treated with trimethylsilyl 2, 2-difluoro-2-fluorosulfonylacetate in the presence of 5 mol % of a Proton Sponge catalyst, the in situ generated difluorocarbene reacted with the dithioesters to afford 2-sulfanylated 1, 1-difluoro-1-alkenes via difluorothiiranes. This reaction can be considered as an electrophilic counterpart of the Wittig-type difluoromethylidenation of carbonyl compounds with nucleophilic difluoromethylene ylides.
EXOCYCLIZATION OF NOVEL β,β-DIFLUORO-α-PHENYLVINYL SULFIDE WITH BIDENTATE HETEROATOM(N,O,S) NUCLEOPHILES
Kim, Bum Tae,Min, Yong Ki,Park, No Kyun,Cho, Kwang Yun,Jeong, In Howa
, p. 641 - 646 (2007/10/02)
The exocyclization of novel β,β-difluoro-α-phenylvinyl sulfide with bidentate heteroatom (N, O, S) nucleophiles afforded various types of heterocyclic ketene acetals (O,O-, O,S-, S,S-, N,N-, N,O-, N,S-).The ease of exocyclization depended on the ring size