130537-02-9Relevant academic research and scientific papers
Copper-Catalyzed Stereoselective Defluorinative Borylation and Silylation of gem-Difluoroalkenes
Tan, Dong-Hang,Lin,Ji, Wei-Wei,Zeng, Yao-Fu,Fan, Wen-Xin,Li, Qingjiang,Gao, Hui,Wang, Honggen
, p. 1032 - 1037 (2018/01/27)
The copper-catalyzed stereoselective defluorinative borylation and silylation of gem-difluoroalkenes was developed. The protocol led to the exclusive formation of Z type monofluoroalkenyl borons and silanes in generally good efficiency with broad substrat
Stereoselective cyanation of β-bromo-β-fluorostyrenes using potassium cyanide and promoted by (CH3CN)4Cu+ BF4-
Eddarir, Said,Kajjout, Mohammed,Rolando, Christian
experimental part, p. 603 - 607 (2012/01/14)
A general method for the synthesis of α-fluorocinnamonitrile based on the stereoselective reaction between β-bromo-β-fluorostyrene and potassium cyanide, promoted by (CH3CN)4Cu+ BF4- in 1-methyl-2-pyr
Fluoro-Julia olefination as a mild, high-yielding route to α-fluoro acrylonitriles
Del Solar, Maria,Ghosh, Arun K.,Zajc, Barbara
experimental part, p. 8206 - 8211 (2009/04/11)
(Chemical Equation Presented) Synthesis of a novel, stable reagent (1,3-benzothiazol-2-ylsulfonyl)fluoroacetonitrile from readily synthesized ethyl α-(1,3-benzothiazol-2-ylsulfanyl)-α-fluoroacetate is reported. Aldehydes undergo condensations with (1,3-be
Preparation of Fluoralkenes from Fluoroacetonitrile
Patrick, Timothy B.,Nadji, Sourena
, p. 147 - 150 (2007/10/02)
A fluorocyanophosphate prepared from fluoroacetonitrile at low temperature reacts with aromatic aldehydes in a modified Wittig procedure to give fluorocyanoalkenes in moderate yield.
