propargylic

propargylic
Describing a saturated carbon atom in a molecule adjacent to a triple bond

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  • Nicholas reaction — The Nicholas reaction is an organic reaction where a dicobalt octacarbonyl stabilized propargylic cation is reacted with a nucleophile. Oxidative demetallation gives the desired alkylated alkyne.[1][2] Several reviews have been published …   Wikipedia

  • Barbier reaction — The Barbier reaction is an organic reaction between an alkyl halide and a carbonyl group as an electrophilic substrate in the presence of aluminium, zinc, indium, tin or its salts. The reaction product is a secondary or tertiary alcohol. The… …   Wikipedia

  • Gold(III) bromide — Gold(III) bromide …   Wikipedia

  • Aluminium hydride — Chembox new ImageFile = ImageSize = IUPACName = aluminium trihydride alumane trihydridoaluminium OtherNames = Aluminium(III) hydride; alane; aluminum hydride, α alane Section1 = Chembox Identifiers CASNo = 7784 21 6 PubChem = SMILES = Section2 =… …   Wikipedia

  • Propiolic — Pro pi*ol ic, a. [Propionic + tetrolic.] (Chem.) Pertaining to, or designating, an organic acid (called also propargylic acid) of the acetylene or tetrolic series, analogous to propionic acid, and obtained as a white crystalline substance. [1913… …   The Collaborative International Dictionary of English

  • Manganese dioxide — Manganese dioxide …   Wikipedia

  • Ene reaction — The Ene reaction (also known as the Alder ene reaction) is a chemical reaction between an alkene with an allylic hydrogen (the ene) and a compound containing a multiple bond (the enophile), in order to form a new σ bond with migration of the ene… …   Wikipedia

  • Noncovalent solid-phase organic synthesis — or NC SPOS is a form of Solid phase synthesis whereby the organic substrate is bonded to the solid phase not by a covalent bond but by other chemical interactions. This bond may consist of an induced dipole interaction between a hydrophobic… …   Wikipedia

  • Overman rearrangement — The Overman rearrangement is a chemical reaction that can be described as a Claisen rearrangement of allylic alcohols to give allylic trichloroacetamides through an imidate intermediate.[1][2][3] The Overman rearrangement was discovered in 1974… …   Wikipedia

  • Propiolic acid — Chembox new Name = Propiolic acid ImageFile = Propiolic acid.png ImageName = IUPACName = 2 Propynoic acid OtherNames = Propiolic acid Acetylene carboxylic acid Propargylic acid Section1 = Chembox Identifiers CASNo = 471 25 0 SMILES = C#CC(=O)O… …   Wikipedia

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