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 (Tschugaeff Olefin Synthesis) L. Chugaev (Tschugaeff), Ber. 32, 3332 (1899). Formation of olefins from alcohols without rearrangement t

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 Synthesis A. E. Chichibabin, J. Russ. Phys. Chem. Soc. 37, 1229 (1906); J. Prakt. Chem. 107, 122 (1924). Condensation of carbonyl compounds

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 (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 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 (Carbylamine Reaction) A. W. Hofmann, Ann. 146, 107 (1868); Ber. 3, 767 (1870). Formation of isonitriles by the reaction of

Cannizzaro Reaction S. Cannizzaro, Ann. 88, 129 (1853); K. List, H. Limpricht, Ann. 90, 180 (1854). Base-catalyzed disproportionation reaction of aromat

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 J. Hoch, Compt. Rend. 198, 1865 (1934); K. N. Campbell, J. F. McKenna, J. Org. Chem. 4, 198 (1939). Formation of aziri

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 P. Fritsch, Ann. 279, 319 (1894); W. P. Buttenberg, ibid. 327; H. Wiechell, ibid. 332. Carbene-mediated rearra

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 E. Buchner, T. Curtius, Ber. 18, 2371 (1885); F. Schlotterbeck, Ber. 40, 479 (1907); 42, 2559 (1909). Formation o

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 E. Paterno, G. Chieffi, Gazz. Chim. Ital. 39, 341 (1909); G. Büchi et al., J. Am. Chem. Soc. 76, 4327 (1954). Formation

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 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 A. Einhorn et al., Ann. 343, 229 (1905); K. Brunner, Ber. 47, 2671 (1914); Monatsh. 36, 509 (1915). Formation of substituted 1,