1375415-67-0Relevant academic research and scientific papers
Stereoselective hydrofluorination of ynamides: A straightforward synthesis of novel α-fluoroenamides
Compain, Guillaume,Jouvin, Kevin,Martin-Mingot, Agnes,Evano, Gwilherm,Marrot, Jerome,Thibaudeau, Sebastien
supporting information; experimental part, p. 5196 - 5198 (2012/06/01)
α-Fluoroenamides, potent rigid fluorinated bioisosters of ureas, have been synthesized by a highly regio- and stereo-selective hydrofluorination of ynamides in anhydrous HF. This reaction provides the first general entry to α-fluoroenamides and can easily be applied to a wide range of substrates.
Copper-mediated selective cross-coupling of 1,1-dibromo-1-alkenes and heteronucleophiles: Development of general routes to heterosubstituted alkynes and alkenes
Jouvin, Kevin,Coste, Alexis,Bayle, Alexandre,Legrand, Frederic,Karthikeyan, Ganesan,Tadiparthi, Krishnaji,Evano, Gwilherm
, p. 7933 - 7947 (2013/01/16)
Efficient and general procedures for the cross-coupling of 1,1-dibromoalkenes and N-, O-, and P-nucleophiles are reported. Fine-tuning of the reaction conditions allows for either site-selective, double, or alkynylative cross-coupling, therefore providing
