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Chemical Reaction - Basic Chemical -

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  • Frankland Synthesis
  • Frankland Synthesis E. Frankland, Ann. 71, 213 (1849); 85, 3641 (1853). Synthesis of zinc dialkyls from alkyl halides and zinc:
  • Franchimont Reaction
  • Franchimont Reaction A. P. N. Franchimont, Ber. 5, 1048 (1872). Carboxylic acid dimerization to 1,2-dicarboxylic acids by treating α-bromocarboxyl
  • Forster Reaction
  • Forster Reaction M. O. J. Forster, J. Chem. Soc. 75, 934 (1899); H. Decker, P. Becker, Ann. 395, 362 (1913). Formation of secondary amines by condensati
  • Forster Diazoketone Synthesis
  • Forster Diazoketone Synthesis M. O. J. Forster, J. Chem. Soc. 107, 260 (1915). Formation of diazoketones from α-oximinoketones by reaction with ch
  • Flood Reaction
  • Flood Reaction E. A. Flood, J. Am. Chem. Soc. 55, 1735 (1933). Formation of trialkylsilyl halides from hexaalkyldisiloxanes using concentrated sulfuric
  • Wurtz-Fittig Reaction
  • Wurtz-Fittig Reaction B. Tollens, R. Fittig, Ann. 131, 303 (1864); R. Fittig, J. König, ibid. 144, 277 (1867). Formation of alkylated aromatic hydr
  • Fischer-Tropsch Syntheses
  • Fischer-Tropsch Syntheses; Synthol Process; Oxo Synthesis F. Fischer, H. Tropsch, Ber. 56, 2428 (1923). Synthesis of hydrocarbons, aliphatic alcohols, a
  • Fischer-Speier Esterification Method
  • Fischer-Speier Esterification Method E. Fischer, A. Speier, Ber. 28, 3252 (1895). Esterification of acids by refluxing with excess alcohol in the presen
  • Fischer-Hepp Rearrangement
  • Fischer-Hepp Rearrangement (Nitrosamine Rearrangement) O. Fischer, E. Hepp, Ber. 19, 2991 (1886). Rearrangement of secondary aromatic nitrosamines to p-
  • Fischer Phenylhydrazone and Osazone Reaction
  • Fischer Phenylhydrazone and Osazone Reaction E. Fischer, Ber. 17, 579 (1884). Formation of phenylhydrazones and osazones by heating sugars with phenylhy
  • Fischer Phenylhydrazine Synthesis
  • Fischer Synthesis E. Fischer, Ber. 8, 589 (1875). Formation of arylhydrazines by reduction of diazo compounds with excess sodium sulfite and hydrolysis
  • Fischer Peptide Synthesis
  • Fischer Peptide Synthesis E. Fischer, Ber. 36, 2982 (1903). Formation of polypeptides by treatment of an α-chloro or α-bromo acyl chloride w
  • Fischer Oxazole Synthesis
  • Fischer Synthesis E. Fischer, Ber. 29, 205 (1896). Condensation of equimolar amounts of aldehyde cyanohydrins and aromatic aldehydes in dry ether in th
  • Fischer Indole Synthesis
  • Fischer Synthesis E. Fischer, F. Jourdan, Ber. 16, 2241 (1883); E. Fischer, O. Hess, ibid. 17, 559 (1884). Formation of indoles on heating aryl hydrazo
  • Kiliani-Fischer Synthesis
  • Kiliani-Fischer Synthesis H. Kiliani, Ber. 18, 3066 (1885); E. Fischer, ibid. 22, 2204 (1889). Extension of the carbon atom chain of aldoses by treatmen
  • Houben-Fischer Synthesis
  • Houben-Fischer Synthesis J. Houben, W. Fischer, J. Prakt. Chem. [2] 123, 89, 262, 313 (1929). Formation of aromatic nitriles by basic hydrolysis of tric
  • Reissert Reaction
  • Reissert Reaction (Grosheintz-Fischer-Reissert Aldehyde Synthesis) A. Reissert, Ber. 38, 1603, 3415 (1905); J. M. Grosheintz, H. O. L. Fischer, J. Am. Chem. Soc. 63, 2021
  • Finkelstein Reaction
  • Finkelstein Reaction H. Finkelstein, Ber. 43, 1528 (1910). Reaction of alkyl halides with sodium iodide in acetone:
  • Ferrier Rearrangement
  • Ferrier Rearrangement R. J. Ferrier, J. Chem. Soc. Perkin Trans. I 1979, 1455. The stereochemically controlled conversion of hex-5-enopyranosides into c
  • Fenton Reaction
  • Fenton Reaction H. J. H. Fenton, Proc. Chem. Soc. 9, 113 (1893); J. Chem. Soc. 65, 899 (1894). Oxidation of α-hydroxy acids with hydrogen peroxide
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