2-allylperfluorocyclobutanone 、 alkaline earth salt of/the/ methylsulfuric acid 以
various solvent(s) 为溶剂,
反应 0.25h,
以22%的产率得到2-(allyl)-1-methyleneperfluorocyclobutene
参考文献:
名称:
Energetics of Fluoroalkene Double Bond Isomerizations
摘要:
The effects of perfluorination of cyclic and acyclic alkenes have been examined. Quantum mechanical calculations and experimental data show that vicinally substituted acyclic alkenes are strongly destabilized by fluorination. Quite surprisingly, the destabilization is much smaller for cyclic analogs. This difference has dramatic consequences for the relative stabilities of double bond isomers in cyclic and acyclic systems, including keto-enol systems. The reasons for the contrast are discussed in detail.
Copolymerizable fluorinated compounds, a process for their preparation
申请人:Bayer Aktiengesellschaft
公开号:US05313003A1
公开(公告)日:1994-05-17
A 2-allyl-perfluoroalkyl-trifluorovinyl ether of the formula ##STR1## wherein R.sup.1.sub.F and R.sup.2.sub.F represent either --CF.sub.3 or, together, (CF.sub.2).sub.n where n=2 or 3.
Energetics of Fluoroalkene Double Bond Isomerizations
作者:Patrick E. Lindner、David M. Lemal
DOI:10.1021/ja963789f
日期:1997.4.1
The effects of perfluorination of cyclic and acyclic alkenes have been examined. Quantum mechanical calculations and experimental data show that vicinally substituted acyclic alkenes are strongly destabilized by fluorination. Quite surprisingly, the destabilization is much smaller for cyclic analogs. This difference has dramatic consequences for the relative stabilities of double bond isomers in cyclic and acyclic systems, including keto-enol systems. The reasons for the contrast are discussed in detail.