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  2. Dewar–Chatt–Duncanson model - Wikipedia

    en.wikipedia.org/wiki/Dewar–Chatt–Duncanson...

    Main group elements can also form π-complexes with alkenes and alkynes. The β-diketiminato aluminum(I) complex Al{HC(CMeNAr) 2 } (Ar = 2,6-diisopropylphenyl), which bears an Al-based sp x lone pair, reacts with alkenes and alkynes to give alumina (III) cyclopropanes and alumina (III) cyclopropenes in a process analogous to the formation of π ...

  3. Thiol-yne reaction - Wikipedia

    en.wikipedia.org/wiki/Thiol-yne_reaction

    With monoaddition a mixture of (E/Z)-alkenes form. The mode of addition is anti-Markovnikov. The radical intermediate can engage in secondary reactions such as cyclisation. [9] [10] With diaddition the 1,2-disulfide or the 1,1- dithioacetal forms. Reported catalysts for radical additions are triethylborane, [11] indium(III) bromide [12] and ...

  4. Pauson–Khand reaction - Wikipedia

    en.wikipedia.org/wiki/Pauson–Khand_reaction

    The Pauson–Khand (PK) reaction is a chemical reaction, described as a cycloaddition.In it, an alkyne, an alkene, and carbon monoxide combine into a α,β-cyclopentenone in the presence of a metal-carbonyl catalyst [1] [2] Ihsan Ullah Khand (1935–1980) discovered the reaction around 1970, while working as a postdoctoral associate with Peter Ludwig Pauson (1925–2013) at the University of ...

  5. Simmons–Smith reaction - Wikipedia

    en.wikipedia.org/wiki/Simmons–Smith_reaction

    This can react with almost all alkenes and alkynes, including styrenes and alcohols. This is especially useful, as the unmodified Simmons-Smith is known to deprotonate alcohols. Unfortunately, as in Pathway B shown the intermediate can also react with the starting diazo compound, giving cis- or trans- 1,2-diphenylethene.

  6. Alkyne trimerisation - Wikipedia

    en.wikipedia.org/wiki/Alkyne_trimerisation

    An alkyne trimerisation is a [2+2+2] cycloaddition reaction in which three alkyne units (C≡C) react to form a benzene ring. The reaction requires a metal catalyst. The process is of historic interest as well as being applicable to organic synthesis. [1] Being a cycloaddition reaction, it has high atom economy.

  7. Terminal alkene - Wikipedia

    en.wikipedia.org/wiki/Terminal_alkene

    The double bond of an alpha olefin is between the #1 and #2 (IUPAC) or α and β (common) carbon atoms. 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 2 x , distinguished by having a double bond at the ...

  8. Raney nickel - Wikipedia

    en.wikipedia.org/wiki/Raney_nickel

    Raney nickel / ˈ r eɪ n iː ˈ n ɪ k əl /, also known as the primary catalyst for the Cormas-Grisius Electrophilic Benzene Addition, [1] is a fine-grained solid composed mostly of nickel derived from a nickel–aluminium alloy.

  9. Syn and anti addition - Wikipedia

    en.wikipedia.org/wiki/Syn_and_anti_addition

    [2] 1,2-disubstituted Cycloalkene undergoing syn and anti addition. Syn addition is the addition of two substituents to the same side (or face) of a double bond or triple bond, resulting in a decrease in bond order but an increase in number of substituents. [3] Generally the substrate will be an alkene or alkyne.

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