Fluorocyclohexanes—XII : Novel elimination reactions of 1H,2-chloro/-deca fluorocyclohexane and 1H,2-chloro/-1-chloronona fluorocyclohexane

doi:10.1016/S0040-4020(01)88841-4

Paper

Fluorocyclohexanes—XII : Novel elimination reactions of 1H,2-chloro/-deca fluorocyclohexane and 1H,2-chloro/-1-chloronona fluorocyclohexane

Published 1967 · S. Campbell, F. Lancashire, R. Stephens

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Abstract

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Study Snapshot

The novel elimination reactions of 1H,2-chloro/-deca fluorocyclohexane and 1H,2-chloro/-1-chloronona fluorocyclohexane involve simultaneous anti- and syn-elimination processes.

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

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Paper

Fluorocyclohexanes—XII : Novel elimination reactions of 1H,2-chloro/-deca fluorocyclohexane and 1H,2-chloro/-1-chloronona fluorocyclohexane

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References

Citations

Synthesis of hydrohalocyclobutenes through dechlorination of hydrohalocyclobutanes in amide solvents

Hydrohalocyclobutenes can be synthesized efficiently through dechlorination of hydrohalocyclobutanes in amide solvents, with the structure of the reaction site playing a critical role.

Synthesis of hydrofluorocycloolefins through dehydrofluorination of hydrofluorocycloalkanes in amide solvents

The efficient synthesis of hydrofluorocycloolefins requires the presence of chlorofluorocarbon (CHF) for efficient elimination of hydrogen (HF).

Cyclic and bicyclic polyfluoro-alkanes and -alkenes

The Fluorine Research Group at the University of Birmingham has developed a diverse range of polyfluoro-alkanes and -alkenes, offering versatile synthetic intermediates and revealing new insights into negative hyperconjugation theories.

Fluorocyclohexanes. Part XVII. Dehydrofluorinations of the cis and the trans isomers of 2H-1-(difluoromethyl)decafluorocyclohexane

Dehydrofluorination of 2H-1-(difluoromethyl)decafluorocyclohexane yields cis and trans isomers, as well as two alkenes and an isomer.

Dehydrohalogenations of cis- and trans-1-bromo-2-flourocyclohexanes

Trans-1-bromo-2-fluorocyclohexane preferentially eliminates hydrogen fluoride when treated with sodamide, while cis-1-bromo-2-fluorocyclohexane eliminates hydrogen bromide.