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  2. Alkenylaluminium compounds - Wikipedia

    en.wikipedia.org/wiki/Alkenylaluminium_compounds

    Hydroaluminations of terminal alkynes typically produce terminal alkenylalanes as a result. Selectivity in hydroaluminations of internal alkynes is typically low, unless an electronic bias exists in the substrate (such as a phenyl ring in conjugation with the alkyne).

  3. Alkyne - Wikipedia

    en.wikipedia.org/wiki/Alkyne

    Terminal alkynes have the formula RC≡CH, where at least one end of the alkyne is a hydrogen atom. An example is methylacetylene (propyne using IUPAC nomenclature). They are often prepared by alkylation of monosodium acetylide. [4] Terminal alkynes, like acetylene itself, are mildly acidic, with pK a values of around 25.

  4. Terminal alkene - Wikipedia

    en.wikipedia.org/wiki/Terminal_alkene

    In organic chemistry, terminal alkenes (alpha-olefins, α-olefins, or 1-alkenes) are a family of organic compounds which are alkenes (also known as olefins) with a chemical formula C x H 2x, distinguished by having a double bond at the primary, alpha (α), or 1-position. [1]

  5. Vinyl iodide functional group - Wikipedia

    en.wikipedia.org/wiki/Vinyl_iodide_functional_group

    Introducing an α-vinyl iodide from a terminal position of an alkyne is a difficult step. in addition, the vinyl metal intermediate can be mildly nucleophilic, for example vinyl aluminum, can form C-C bonds under catalytic conditions.

  6. Alkynylation - Wikipedia

    en.wikipedia.org/wiki/Alkynylation

    In organic chemistry, alkynylation is an addition reaction in which a terminal alkyne (−C≡CH) is added to a carbonyl group (C=O) to form an α-alkynyl alcohol (R 2 C(−OH)−C≡C−R). [1] [2] When the acetylide is formed from acetylene (HC≡CH), the reaction gives an α-ethynyl alcohol. This process is often referred to as ethynylation.

  7. 1-Butyne - Wikipedia

    en.wikipedia.org/wiki/1-Butyne

    It is a terminal alkyne. The compound is a common terminal alkyne substrate in diverse studies of catalysis. It is a colorless combustible gas. [1] 1-Butyne participates in reactions typical for terminal alkynes, such as alkyne metathesis, [2] hydrogenation, condensation with formaldehyde.

  8. Crabbé reaction - Wikipedia

    en.wikipedia.org/wiki/Crabbé_reaction

    The Crabbé reaction (or Crabbé allene synthesis, Crabbé–Ma allene synthesis) is an organic reaction that converts a terminal alkyne and aldehyde (or, sometimes, a ketone) into an allene in the presence of a soft Lewis acid catalyst (or stoichiometric promoter) and secondary amine.

  9. 1-Decyne - Wikipedia

    en.wikipedia.org/wiki/1-Decyne

    1-Decyne is the organic compound with the formula C 8 H 17 C≡CH. It is a terminal alkyne.A colorless liquid, 1-decyne is used as a model substrate when evaluating methodology in organic synthesis.