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There is a page named "Tosylhydrazone" on Wikipedia

  • A tosylhydrazone in organic chemistry is a functional group with the general structure RR'C=N-NH-Ts where Ts is a tosyl group. Organic compounds having...
    5 KB (657 words) - 19:40, 27 October 2022
  • Thumbnail for Bamford–Stevens reaction
    Bamford–Stevens reaction is a chemical reaction whereby treatment of tosylhydrazones with strong base gives alkenes. It is named for the British chemist...
    14 KB (1,481 words) - 16:52, 26 October 2023
  • catecholborane to reduce α,β-unsaturated tosylhydrazones. The mechanism of NaBH3CN reduction of α,β-unsaturated tosylhydrazones has been examined using deuterium-labeling...
    40 KB (4,211 words) - 13:40, 13 February 2024
  • The Shapiro reaction or tosylhydrazone decomposition is an organic reaction in which a ketone or aldehyde is converted to an alkene through an intermediate...
    10 KB (1,020 words) - 02:35, 25 May 2024
  • Thumbnail for Diazomethane
    Organic Syntheses; Collected Volumes, vol. 8, p. 612. X. Creary (1990). "Tosylhydrazone Salt Pyrolyses: Phenydiazomethanes". Organic Syntheses; Collected Volumes...
    18 KB (1,648 words) - 12:49, 4 July 2024
  • Thumbnail for Alkene
    single ketone can also be converted to the corresponding alkene via its tosylhydrazone, using sodium methoxide (the Bamford–Stevens reaction) or an alkyllithium...
    48 KB (5,122 words) - 23:58, 18 July 2024
  • doi:10.1351/goldbook.H02879 Shapiro, Robert H. (1976). "Alkenes from Tosylhydrazones". Org. React. 23 (3): 405–507. doi:10.1002/0471264180.or023.03. ISBN 0471264180...
    5 KB (446 words) - 21:32, 10 December 2023
  • Thumbnail for Carbonyl reduction
    Wolff-Kishner reaction. The Caglioti modification, for instance, uses tosylhydrazone with a hydride donor in milder conditions with no base; the Myers modification...
    24 KB (2,715 words) - 12:53, 24 June 2024
  • Thumbnail for Ketene
    the carbonylation of α‐diazocarbonyl compounds and a variety of N‐tosylhydrazones catalysed by Co(II)–porphyrin metalloradicals leading to the formation...
    11 KB (1,294 words) - 18:49, 13 July 2024
  • Thumbnail for Organolithium reagent
    reaction, two equivalents of strong alkyllithium base react with p-tosylhydrazone compounds to produce the vinyllithium, or upon quenching, the olefin...
    55 KB (5,971 words) - 20:35, 22 July 2024
  • bistrimethylsilylpropynone 1 by reaction with p-toluenesulfonylhydrazide to tosylhydrazone 2 followed by treatment with sodium cyanoborohydride to allene 3 and...
    3 KB (272 words) - 19:20, 14 December 2023
  • Thumbnail for Abeo-HHC acetate
    THC-O-acetate Srebnik M, Mechoulam R (1984). "Reactions of cannabinoid tosylhydrazones: Stereochemical aspects". Tetrahedron. 40 (19): 3839–3843. doi:10...
    2 KB (122 words) - 06:48, 14 April 2024
  • Diazo compounds are intermediates in the Bamford–Stevens reaction of tosylhydrazones to alkenes, again with a carbene intermediate: In the Doyle–Kirmse...
    13 KB (1,439 words) - 01:23, 17 July 2024