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acetylenic ketone

См. также в других словарях:

  • organosulfur compound — ▪ chemical compound Introduction also spelled  organosulphur compound , also called  organic sulfur compound   a subclass of organic substances that contain sulfur and that are known for their varied occurrence and unusual properties. They are… …   Universalium

  • Jones oxidation — The Jones oxidation is a chemical reaction described as the chromic acid oxidation of primary and secondary alcohols to carboxylic acids and ketones, respectively. [cite journal | author = Bowden, K.; Heilbron, I. M.; Jones, E. R. H | journal = J …   Wikipedia

  • Progesterone — Systematic (IUPAC) name Pregn 4 ene 3,20 dione …   Wikipedia

  • Metal acetylide — A metal acetylide is an alkyne for which the terminal proton (hydrogen) has been replaced by a metal such as sodium or an organolithium. So, for example, the alkyne CH3C≡CH could be deprotonated to form the acetylide ion CH3C≡C−. Once it has been …   Wikipedia

  • steroid — /stear oyd, ster /, Biochem. n. 1. any of a large group of fat soluble organic compounds, as the sterols, bile acids, and sex hormones, most of which have specific physiological action. adj. 2. Also, steroidal /sti royd l, ste /. pertaining to or …   Universalium

  • Eschenmoser fragmentation — The Eschenmoser fragmentation (also called the Eschenmoser Tanabe fragmentation) is the chemical reaction of α,β epoxyketones (1) with aryl sulfonylhydrazines (2) to give alkynes (3) and carbonyl compounds (4). [cite journal | author = A.… …   Wikipedia

  • Meyer-Schuster rearrangement — The Meyer Schuster rearrangement is the chemical reaction described as an acid catalyzed rearrangement of propargyl alcohols to α,β unsaturated ketones.Ref|Meyer1922Ref|Swaminathan1971Ref|Vartanyan1967Acid catalysts can include acetic acid,… …   Wikipedia

  • Acetylide — Identifiers ChemSpider 6113  Y Jmol 3D images …   Wikipedia

  • Meyer–Schuster rearrangement — The Meyer Schuster rearrangement is the chemical reaction described as an acid catalyzed rearrangement of secondary and tertiary propargyl alcohols to α,β unsaturated ketones if the alkyne group is internal and α,β unsaturated aldehydes if the… …   Wikipedia

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