Kazia, AK; Melngaile, RM; Mishnev, AM; Veliks, JV in [Kazia, Armands; Melngaile, Renate; Mishnev, Anatoly; Veliks, Janis] Latvian Inst Organ Synth, Aizkraukles 21, LV-1006 Riga, Latvia published Johnson-Corey-Chaykovsky fluorocyclopropanation of double activated alkenes: scope and limitations in 2020.0, Cited 44.0. Name: 3-Pyridinecarboxaldehyde. The Name is 3-Pyridinecarboxaldehyde. Through research, I have a further understanding and discovery of 500-22-1.
Johnson-Corey-Chaykovsky fluorocyclopropanation of double activated alkenes utilizing S-monofluoromethyl-S-phenyl-2,3,4,5-tetramethylphenylsulfonium tetrafluoroborate is an efficient approach to obtain a range of monofluorocyclopropane derivatives. So far, fluoromethylsulfonium salts have displayed the broadest scope for direct fluoromethylene transfer. In contrast to more commonly used fluorohalomethanes or freon derivatives, diarylfluoromethylsulfonium salts are bench stable, easy-to use reagents useful for the direct transfer of a fluoromethylene group to alkenes giving access to the challenging products – fluorocyclopropane derivatives. Interplay between the reactivity of the starting materials and stability of the fluorocyclopropanes formed determines the outcome of the process.
Name: 3-Pyridinecarboxaldehyde. About 3-Pyridinecarboxaldehyde, If you have any questions, you can contact Kazia, AK; Melngaile, RM; Mishnev, AM; Veliks, JV or concate me.
Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem