4927-29-1Relevant academic research and scientific papers
Addition of Nucleophiles to Fluorinated Michael Acceptors
Ramb, Daniel C.,Lerchen, Andreas,Kischkewitz, Marvin,Beutel, Bernd,Fustero, Santos,Haufe, Günter
, p. 1751 - 1759 (2016)
A series of nucleophiles, including primary and secondary amines, primary alcohols, and thiols, as well as diethyl malonate and nitromethane, were added to different fluorinated Michael acceptors including 2-fluoroalk-1-en-3-ones and 2-fluoro-1-phenylprop
A NEW ROUTE TO 2-FLUORO-1-OLEFINS UTILIZING A SYNTHETIC EQUIVALENT FOR THE 1-FLUOROETHENE ANION
Matthews, Donald P.,Gross, Raymond S.,McCarthy, James R.
, p. 1027 - 1030 (1994)
The preparation of (E)-tributyl(1-fluoro-2-trimethylsilyl)vinylstannane (10), a synthetic equivalent for the 1-fluoroethene anion, and its utility for the synthesis of nucleoside 20, and other 2-fluoro-1-olefins is described.
Difluorohomologation of ketones
Kosobokov, Mikhail D.,Levin, Vitalij V.,Struchkova, Marina I.,Dilman, Alexander D.
supporting information, p. 760 - 763 (2015/03/05)
A method for the homologation of ketones with the CF2 fragment is described. The reaction involves silylation, room-temperature difluorocyclopropanation of silyl enol ethers, and selective ring opening of cyclopropanes under acidic conditions. The whole three-step sequence is conveniently performed in a one-pot mode.
Sodium bromodifluoroacetate: A difluorocarbene source for the synthesis of gem -difluorocyclopropanes
Oshiro, Kojun,Morimoto, Yoshimichi,Amii, Hideki
scheme or table, p. 2080 - 2084 (2010/08/13)
As a new difluorocarbene source, sodium bromodifluoroacetate (BrCF 2CO2Na) was found to be effective for high-yielding synthesis of gem-difluorocyclopropanes and gem-difluorocyclopropenes under mild conditions. Georg Thieme Verlag Stuttgart.
Fluoroalkylation et annelation de β-dicetones cycliques
Elkik, Elias,Dahan, Rachel,Parlier, Andree
, p. 353 - 360 (2007/10/02)
We describe a general method of preparation of α-fluoro-β-chloro (or bromo) ethylketones 2 by reaction of Grignard reagents with α-fluoro-β-chloro (or bromo) propionic ethyl esters 1 : CH2X-CHF-COOEt (1)+ RMgX R-CO-CHF-CH2X (2); X = Cl, Br; R = alipha
