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  • Gabriel-Colman Rearrangement
  • Gabriel-Colman Rearrangement (Phthalimidoacetic Ester→ Rearrangement, Gabriel Isoquinoline Synthesis) S. Gabriel, J. Colman, Ber. 33, 980, 996, 2630 (1900); 35, 2421
  • Sarett Oxidation
  • Sarett Oxidation; Collins Oxidation G. I. Poos, G. E. Arth, R. E. Beyler, L. H. Sarett, J. Am. Chem. Soc. 75, 422 (1953). Oxidation of primary and secon
  • Clemmensen Reduction
  • Clemmensen Reduction E. Clemmensen, Ber. 46, 1837 (1913); 47, 51, 681 (1914). Reduction of carbonyl groups of aldehydes and ketones to methylene groups
  • Leuckart (Leukart) Reaction
  • Leuckart (Leukart) Reaction; Leuckart-Wallach Reaction; Eschweiler-Clarke Reaction R. Leuckart, Ber. 18, 2341 (1885). Reductive alkylation of ammonium (
  • Claisen-Schmidt Condensation
  • Claisen-Schmidt Condensation L. Claisen, A. Claparède, Ber. 14, 2460 (1881); J. G. Schmidt, ibid. 1459. Condensation of an aromatic aldehyde with
  • Claisen Rearrangement
  • Claisen Rearrangement; Eschenmoser-Claisen Rearrangement; Johnson-Claisen Rearrangement; Ireland-Claisen Rearrangement L. Claisen, Ber. 45, 3157 (1912); L. Claisen, E. Tie
  • Darzens Condensation
  • Darzens Condensation (Darzens-Claisen Reaction, Glycidic Ester Condensation) G. Darzens, Compt. Rend. 139, 1214 (1904); 141, 766 (1905); 142, 214 (1906).
  • 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
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