- acetylenic ketone
- кетон ацетиленового ряда
English-Russian dictionary of chemistre. 2014.
English-Russian dictionary of chemistre. 2014.
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Metal acetylide — A metal acetylide is an alkyne for which the terminal proton (hydrogen) has been replaced by a metal such as sodium or an organolithium.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