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Some Recent Results in Organofluorine Chemistry

open access: yesBulletin des Sociétés Chimiques Belges, 1992
André Laurent
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The [2,3]-Wittig rearrangement in organofluorine chemistry

Journal of the Chemical Society, Chemical Communications, 1992
Ethers of a difluoroallylic alcohol undergo clean, high-yielding [2,3]-Wittig rearrangements in tetrahydrofuran (THF) at –30 °C, affording highly functionalised products with an in-chain difluoromethylene group.
Sunita T. Patel, Jonathan M. Percy
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Organofluorine Chemistry: Synthesis and Conformation of Vicinal Fluoromethylene Motifs

The Journal of Organic Chemistry, 2012
The C-F bond is the most polar bond in organic chemistry, and thus the bond has a relatively large dipole moment with a significant -ve charge density on the fluorine atom and correspondingly a +ve charge density on carbon. The electrostatic nature of the bond renders it the strongest one in organic chemistry.
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Editorial (Thematic Issue: Organofluorine Chemistry)

Current Organic Chemistry, 2015

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Organofluorine chemistry

Philosophical Transactions of the Royal Society of London. Series A: Mathematical, Physical and Engineering Sciences, 2000
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A Fruitful Decade of Organofluorine Chemistry: New Reagents and Reactions

CCS Chemistry, 2022
Feng-Ling Qing   +2 more
exaly  

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