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Chemical Reaction - Basic Chemical -

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  • Ciamician-Dennstedt Rearrangement
  • Ciamician-Dennstedt Rearrangement G. L. Ciamician, M. Dennstedt, Ber. 14, 1153 (1881). Expansion of the pyrrole ring by heating with chloroform or other
  • Chugaev Reaction
  • Chugaev Reaction (Tschugaeff Olefin Synthesis) L. Chugaev (Tschugaeff), Ber. 32, 3332 (1899). Formation of olefins from alcohols without rearrangement t
  • Chichibabin Reaction
  • Chichibabin Reaction A. E. Chichibabin, O. A. Zeide, J. Russ. Phys. Chem. Soc. 46, 1216 (1914), C.A. 9, 1901 (1915). Amination of s and other heterocycl
  • Chichibabin Pyridine Synthesis
  • Chichibabin Synthesis A. E. Chichibabin, J. Russ. Phys. Chem. Soc. 37, 1229 (1906); J. Prakt. Chem. 107, 122 (1924). Condensation of carbonyl compounds
  • Chapman Rearrangement
  • Chapman Rearrangement O. Mumm et al., Ber. 48, 379 (1915); A. W. Chapman, J. Chem. Soc. 127, 1992 (1925); 1927, 174; 1929, 569. Thermal rearrangement of
  • Castro-Stephens Coupling
  • Castro-Stephens Coupling (Stephens-Castro Coupling, Castro Reaction) C. E. Castro, R. D. Stephens, J. Org. Chem. 28, 2163 (1963); R. D. Stephens, C. E. Castro, ibid. 3313;
  • Carroll Rearrangement
  • Carroll Rearrangement M. F. Carroll, J. Chem. Soc. 1940, 704; 1941, 507; W. Kimel, A. C. Cope, J. Am. Chem. Soc. 65, 1992 (1943). Preparation of γ
  • Hofmann Isonitrile Synthesis
  • Hofmann Isonitrile Synthesis (Carbylamine Reaction) A. W. Hofmann, Ann. 146, 107 (1868); Ber. 3, 767 (1870). Formation of isonitriles by the reaction of
  • Cannizzaro Reaction
  • Cannizzaro Reaction S. Cannizzaro, Ann. 88, 129 (1853); K. List, H. Limpricht, Ann. 90, 180 (1854). Base-catalyzed disproportionation reaction of aromat
  • Camps Quinoline Synthesis
  • Camps Synthesis R. Camps, Ber. 22, 3228 (1899); Arch. Pharm. 237, 659 (1899); 239, 591 (1901). Formation of hydroxyquinolines from o-acylaminoacetophen
  • Hoch-Campbell Aziridine Synthesis
  • Hoch-Campbell Aziridine Synthesis J. Hoch, Compt. Rend. 198, 1865 (1934); K. N. Campbell, J. F. McKenna, J. Org. Chem. 4, 198 (1939). Formation of aziri
  • Glaser Coupling
  • Glaser Coupling; Eglinton Reaction; Cadiot-Chodkiewicz Coupling C. Glaser, Ber. 2, 422 (1869). Homocoupling of terminal alkynes catalyzed by cuprous sal
  • Fritsch-Buttenberg-Wiechell Rearrangement
  • Fritsch-Buttenberg-Wiechell Rearrangement P. Fritsch, Ann. 279, 319 (1894); W. P. Buttenberg, ibid. 327; H. Wiechell, ibid. 332. Carbene-mediated rearra
  • Buchwald-Hartwig Cross Coupling Reaction
  • Buchwald-Hartwig Cross Coupling Reaction J. Louie, J. F. Hartwig, Tetrahedron Letters 36, 3609 (1995); A. S. Guram et al., Angew. Chem. Int. Ed. 34, 1348 (1995).
  • Buchner-Curtius-Schlotterbeck Reaction
  • Buchner-Curtius-Schlotterbeck Reaction E. Buchner, T. Curtius, Ber. 18, 2371 (1885); F. Schlotterbeck, Ber. 40, 479 (1907); 42, 2559 (1909). Formation o
  • Buchner Method of Ring Enlargement
  • Buchner Method of Ring Enlargement E. Buchner, Ber. 29, 106 (1896); E. Buchner, K. Schottenhammer, Ber. 53, 865 (1920). Diazoacetic acid ester reacts wi
  • Paterno-Büchi Reaction
  • Paterno-Büchi Reaction E. Paterno, G. Chieffi, Gazz. Chim. Ital. 39, 341 (1909); G. Büchi et al., J. Am. Chem. Soc. 76, 4327 (1954). Formation
  • Bucherer Reaction
  • Bucherer Reaction H. T. Bucherer, J. Prakt. Chem.  69, 49 (1904); R. Lepetit, Bull. Soc. Ind. Mulhouse 1903, 326. Reversible formation of β-na
  • Bucherer Carbazole Synthesis
  • Bucherer Synthesis H. T. Bucherer, F. Seyde, J. Prakt. Chem. 77(2), 403 (1908). Formation of carbazoles from naphthols or naphthylamines, aryl hydrazin
  • Einhorn-Brunner Reaction
  • Einhorn-Brunner Reaction A. Einhorn et al., Ann. 343, 229 (1905); K. Brunner, Ber. 47, 2671 (1914); Monatsh. 36, 509 (1915). Formation of substituted 1,
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