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-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 (Schlittler-Müller Modification) C. Pomeranz, Monatsh. 14, 116 (1893); P. Fritsch, Ber. 26, 419 (1893); E. Schlittler, J. Müller, Helv.
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 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 A. W. Hofmann, Ber. 16, 558 (1883); 18, 5, 109 (1885); K. Löffler, C. Freytag, ibid. 42, 3427 (1909). Formati
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 E. Frankland, Ann. 71, 213 (1849); 85, 3641 (1853). Synthesis of zinc dialkyls from alkyl halides and zinc:
Franchimont Reaction A. P. N. Franchimont, Ber. 5, 1048 (1872). Carboxylic acid dimerization to 1,2-dicarboxylic acids by treating α-bromocarboxyl
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 M. O. J. Forster, J. Chem. Soc. 107, 260 (1915). Formation of diazoketones from α-oximinoketones by reaction with ch
Flood Reaction E. A. Flood, J. Am. Chem. Soc. 55, 1735 (1933). Formation of trialkylsilyl halides from hexaalkyldisiloxanes using concentrated sulfuric
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; Synthol Process; Oxo Synthesis F. Fischer, H. Tropsch, Ber. 56, 2428 (1923). Synthesis of hydrocarbons, aliphatic alcohols, a
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 (Nitrosamine Rearrangement) O. Fischer, E. Hepp, Ber. 19, 2991 (1886). Rearrangement of secondary aromatic nitrosamines to p-
Fischer Phenylhydrazone and Osazone Reaction E. Fischer, Ber. 17, 579 (1884). Formation of phenylhydrazones and osazones by heating sugars with phenylhy
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 E. Fischer, Ber. 36, 2982 (1903). Formation of polypeptides by treatment of an α-chloro or α-bromo acyl chloride w
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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