Encyclopedia

  • Herz Reaction

    Herz Reaction R. Herz, DE 360690 (1914 to Cassella & Co.); US 1637023 (1928); US 1699432 (1929). Formation of o-aminothiophenols by heating aromatic

  • HERON Rearrangement

    HERON Rearrangement (Heteroatom Rearrangements on ) J. M. Buccigross et al., Aust. J. Chem. 48, 353 (1995); J. M. Buccigross, S. A. Glover, J. Chem. Soc. Perkin Trans. II

  • Henry Reaction

    Henry Reaction (Nitroaldol Reaction) L. Henry, Compt. Rend. 120, 1265 (1895); J. Kamlet, US 2151517 (1939). Base-catalyzed aldol-type condensation, q.v.

  • Henkel Reaction

    Henkel Reaction (Raecke Process, Henkel Process) B. Raecke, DE 936036 (1952) and DE 958920 (1952) to Henkel & Co. Industrial scale thermal rearrange

  • Hell-Volhard-Zelinsky Reaction

    Hell-Volhard-Zelinsky Reaction C. Hell, Ber. 14, 891 (1881); J. Volhard, Ann. 242, 141 (1887); N. Zelinsky, Ber. 20, 2026 (1887). α-Halogenation o

  • Helferich Method

    Helferich Method B. Helferich, E. Schmitz-Hillebrecht, Ber. 66, 378 (1933). Glycosidation of an acetylated sugar by heating with a phenol in the presenc

  • Heck Reaction

    Heck Reaction R. F. Heck, J. P. Nolley, Jr., J. Org. Chem. 37, 2320 (1972). Stereospecific palladium-catalyzed coupling of alkenes with organic halides

  • Hayashi Rearrangement

    Hayashi Rearrangement M. Hayashi, J. Chem. Soc. 1927, 2516; 1930, 1513, 1520, 1524. Rearrangement of o-benzoylbenzoic acids in the presence of sulfuric

  • Haworth Phenanthrene Synthesis

    Haworth Synthesis R. D. Haworth, J. Chem. Soc. 1932, 1125, 2717, idem et al., ibid. 1784, 2248, 2720; 1934, 454. Preparation of phenanthrenes from naph

  • Haworth Methylation

    Haworth Methylation W. N. Haworth, J. Chem. Soc. 107, 13 (1915). Formation of methylated methyl glycosides from monosaccharides with dimethyl sulfate an

  • Sommelet-Hauser Rearrangement

    Sommelet-Hauser Rearrangement M. Sommelet, Compt. Rend. 205, 56 (1937). Rearrangement of benzyl quaternary ammonium salts to ortho substituted benzyldia

  • Harries Ozonide Reaction

    Harries Ozonide Reaction (Ozonolysis) C. Harries, Ann. 343, 311 (1905). Treatment of olefins with ozone as a method of cleaving olefinic linkages. On hy

  • Hantzsch Pyrrole Synthesis

    Hantzsch Pyrrole Synthesis A. Hantzsch, Ber. 23, 1474 (1890). Formation of pyrrole derivatives from α-chloromethyl ketones, β-keto esters and

  • Hantzsch Dihydropyridine Synthesis

    Hantzsch Synthesis ( Synthesis) A. Hantzsch, Ann. 215, 1, 72 (1882); Ber. 18, 1744 (1885); 19, 289 (1886). Synthesis of dihydropyridines by condensatio

  • Hammick Reaction

    Hammick Reaction P. Dyson, D. L. Hammick, J. Chem. Soc. 1937, 1724. Decarboxylation of α-picolinic or related acids in the presence of carbonyl co

  • Lieben Iodoform Reaction

    Lieben Iodoform Reaction (Haloform Reaction) A. Lieben, Ann. (Suppl.) 7, 218 (1870). Cleavage of methyl ketones with halogens (mostly iodine) and base t

  • Koch-Haaf Carboxylations

    Koch-Haaf Carboxylations H. Koch, Brennstoff Chem. 36, 321 (1955); H. Koch, W. Haaf, Ann. 618, 251 (1958). Formation of tertiary carboxylic acids by tre

  • Vilsmeier-Haack Reaction

    Vilsmeier-Haack Reaction A. Vilsmeier, A. Haack, Ber. 60, 119 (1927). Formylation of activated aromatic or heterocyclic compounds with disubstituted for

  • Gutknecht Pyrazine Synthesis

    Gutknecht Pyrazine Synthesis H. Gutknecht, Ber. 12, 2290 (1879); 13, 1116 (1880). Cyclization of α-amino ketones, produced by reduction of isonitr

  • Guerbet Reaction

    Guerbet Reaction M. Guerbet, Compt. Rend. 128, 511 (1899). Condensation of 1° or 2° alcohols at high temperature and pressure in the presence of

  • Total:464 Page 13 of 24 <<Previous 19 10 11 12 13 14 15 16 17 18 1924 Next>>
  • About|Contact|Cas|Product Name|Molecular|Country|Encyclopedia

    Message|New Cas|MSDS|Service|Advertisement|CAS DataBase|Article Data|Manufacturers | Chemical Catalog

    ©2008 LookChem.com,License: ICP

    NO.:Zhejiang16009103

    complaints:service@lookchem.com Desktop View