hydrocarbon counterpart, perfluoro-2-(trifluoromethyl)propene is a highly reactive compound. It participates in both heterolytic and homolytic reactions. It readily reacts with nucleophiles and sluggishly with electrophiles. It reacts as well with common organic solvents, such as dimethylformamide, ethanol and others. In this communication, we describe its reactions with trifluoromethylthiocopper, sulfur
Dyatkin,B.L. et al., Journal of Organic Chemistry USSR (English Translation), 1973, vol. 9, p. 1810 - 1814
作者:Dyatkin,B.L. et al.
DOI:——
日期:——
Dyatkin, B. L.; Sterlin, S. R.; Zhuravkova, L. G., Zhurnal Organicheskoi Khimii, 1973, vol. 9, p. 1810 - 1814
作者:Dyatkin, B. L.、Sterlin, S. R.、Zhuravkova, L. G.、Martynov, B. I.、Knunyants, I. L.
DOI:——
日期:——
Exchange reactions of organotin and organosilicon compounds with vinylic fluorine
作者:D.I. Rossman、A.J. Muller
DOI:10.1016/s0022-1139(00)82196-x
日期:1993.1
Compounds carrying reactive fluorine atoms, such as methylphosphonic difluoride and perfluoroisobutene, undergo facile exchange with organosilanes and stannanes. Reactions with protic nucleophiles also yield similar products. To account for the products formed and observed reactivity differences, appropriate mechanisms are proposed. The reactions described herein have considerable synthetic utility