Sulfonation of acyclic fluorovinyl ethers

CG Krespan, BE Smart, EG Howard

Index: Krespan,C.G. et al. Journal of the American Chemical Society, 1977 , vol. 99, p. 1214 - 1217

Full Text: HTML

Citation Number: 29

Abstract

Abstract: Contrary to implications in the literature, polyfluorovinyl ethers have been shown to form unstable sultones with sul-fur trioxide. Near 25 OC these sultones isomerize easily to P- carbonylsulfonate esters. A fluorovinyl diether was found to lead preferentially to cyclic sulfate, a convenient precursor to a perfluoro a-diketone. Mechanisms for these transformations are proposed. These reactions offer superior routes to the two classes of ...

Related Articles:

Oxyphosphorane models for displacement reactions of pyrophosphates

[Ramirez,F. et al. Journal of the American Chemical Society, 1974 , vol. 96, p. 2429 - 2433]

Reactions of tetrafluoroethene oligomers part 11 [1] flash vacuum thermolysis of some products derived from the pentamer and hexamer oligomers.

[Coe, Paul L.; Cook, Michael I.; Owen, Ian R. Journal of Fluorine Chemistry, 1989 , vol. 42, p. 389 - 402]

More Articles...