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  2. Diethylaminosulfur trifluoride - Wikipedia

    en.wikipedia.org/wiki/Diethylaminosulfur_trifluoride

    Diethylaminosulfur trifluoride (DAST) is the organosulfur compound with the formula Et 2 NSF 3. This liquid is a fluorinating reagent used for the synthesis of organofluorine compounds . [ 1 ] The compound is colourless; older samples assume an orange colour.

  3. Fluorination with aminosulfuranes - Wikipedia

    en.wikipedia.org/wiki/Fluorination_with_amino...

    Fluorination with aminosulfuranes is a chemical reaction that transforms oxidized organic compounds into organofluorine compounds.Aminosulfuranes selectively exchange hydroxyl groups for fluorine, but are also capable of converting carbonyl groups, halides, silyl ethers, and other functionality into organofluorides.

  4. Organofluorine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organofluorine_chemistry

    Organofluorine compounds are components of liquid crystal displays. The polymeric analogue of triflic acid, nafion is a solid acid that is used as the membrane in most low temperature fuel cells. The bifunctional monomer 4,4'-difluorobenzophenone is a precursor to PEEK-class polymers.

  5. Fluorination by sulfur tetrafluoride - Wikipedia

    en.wikipedia.org/wiki/Fluorination_by_sulfur...

    This was demonstrated in the synthesis of meso-difluorosuccinate from (L)-tartrate and the synthesis of (D)- and (L)-difluorosuccinate from meso-tartrate. [6] Carbonyl compounds generally react with SF 4 to yield geminal difluorides. Reaction times tend to be on the order of hours and yields are moderate. [7]

  6. Organoboron chemistry - Wikipedia

    en.wikipedia.org/wiki/Organoboron_chemistry

    The most-studied class of organoboron compounds has the formula BR n H 3−n. These compounds are catalysts, reagents, and synthetic intermediates. Except a few bulky derivatives, the primary and secondary hydrides (n = 1 or 2) are, like diborane itself, strongly Lewis acidic and dimerize in condensed phases.

  7. Organotin chemistry - Wikipedia

    en.wikipedia.org/wiki/Organotin_chemistry

    Organotin chemistry is the scientific study of the synthesis and properties of organotin compounds or stannanes, which are organometallic compounds containing tin–carbon bonds. The first organotin compound was diethyltin diiodide ( (CH 3 CH 2 ) 2 SnI 2 ), discovered by Edward Frankland in 1849. [ 1 ]

  8. Carbones - Wikipedia

    en.wikipedia.org/wiki/Carbones

    The structure of carbodicarbenes greatly resembles that of carbodiphosphoranes. [4] Computational data for a N-methyl-substituted carbodicarbene predicted a carbon-carbon bond with a length only marginally longer than a C=C bond in a typical allene at 1.358 Å (compared with 1.308 Å for allene), but with a significantly bent bond angle of 131.8° (compared to 180° for a standard linear ...

  9. Organic synthesis - Wikipedia

    en.wikipedia.org/wiki/Organic_synthesis

    Organic compounds are molecules consisting of combinations of covalently-linked hydrogen, carbon, oxygen, and nitrogen atoms. Within the general subject of organic synthesis, there are many different types of synthetic routes that can be completed including total synthesis, [1] stereoselective synthesis, [2] automated synthesis, [3] and many ...