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  • Gabriel Synthesis
  • Gabriel Synthesis S. Gabriel, Ber. 20, 2224 (1887). Conversion of alkyl halides to primary amines by treatment with potassium phthalimide and subsequent
  • Gabriel Ethylenimine Method
  • Gabriel Ethylenimine Method (Gabriel-Marckwald Ethylenimine Synthesis) S. Gabriel et al., Ber. 21, 1049 (1888); W. Marckwald et al., ibid. 32, 2036 (1899); 33, 764 (1900);
  • Pomeranz-Fritsch Reaction
  • Pomeranz-Fritsch Reaction (Schlittler-Müller Modification) C. Pomeranz, Monatsh. 14, 116 (1893); P. Fritsch, Ber. 26, 419 (1893); E. Schlittler, J. Müller, Helv.
  • Fries Rearrangement
  • Fries Rearrangement K. Fries, G. Fink, Ber. 41, 4271 (1908); K. Fries, W. Pfaffendorf, ibid. 43, 212 (1910). Rearrangement of phenolic esters to o- and/
  • Friedlaender Synthesis
  • Friedlaender Synthesis P. Friedlaender, Ber. 15, 2572 (1882); P. Friedlaender, C. F. Gohring, ibid. 16, 1833 (1883). Base-catalyzed condensation of 2-am
  • Hofmann-Löffler-Freytag Reaction
  • Hofmann-Löffler-Freytag Reaction A. W. Hofmann, Ber. 16, 558 (1883); 18, 5, 109 (1885); K. Löffler, C. Freytag, ibid. 42, 3427 (1909). Formati
  • Freund Reaction
  • Freund Reaction; Gustavson Reaction; Hass Process A. Freund, Monatsh. 3, 625 (1882); G. Gustavson, J. Prakt. Chem. [2] 36, 300 (1887); H. B. Hass et al., Ind. Eng. Chem.
  • 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
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