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  • 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,
  • Maillard Reaction
  • Maillard Reaction (“Browning”Reaction) L. C. Maillard, Compt. Rend. 154, 66 (1912); Ann. Chim. 9, 5, 258 (1916). The reactions of amino grou
  • Brook Rearrangement
  • Brook Rearrangement A. G. Brook, J. Am. Chem. Soc. 80, 1886 (1958); idem et al., ibid. 81, 981 (1959). Base-catalyzed silicon migration from carbon to o
  • Bradsher Reaction
  • Bradsher Reaction C. K. Bradsher, J. Am. Chem. Soc. 62, 486 (1940). Acid-catalyzed cyclodehydration of o-acyldiarylmethanes to anthracene derivatives:
  • Bradsher Cyclization
  • Bradsher Cyclization (Bradsher Cycloaddition) C. K. Bradsher, T. W. G. Solomons, J. Am. Chem. Soc. 80, 933 (1958). [4 + 2] addition of a common dienophi
  • Boyland-Sims Oxidation
  • Boyland-Sims Oxidation E. Boyland et al., J. Chem. Soc. 1953, 3623; E. Boyland, P. Sims, ibid. 1954, 980. Alkaline persulfate oxidation of aromatic amin
  • Bouveault Aldehyde Synthesis
  • Bouveault Aldehyde Synthesis L. Bouveault, Bull. Soc. Chim. France 31, 1306, 1322 (1904). Action of Grignard or organic lithium reagents on N,N-disubsti
  • Wolffenstein-Böters Reaction
  • Wolffenstein-Böters Reaction O. Böters, R. Wolffenstein, DE 194883 (1906); FR 380121 (1907); GB 17521 (1907); US 923761 (1909). Simultaneous o
  • Borsche-Drechsel Cyclization
  • Borsche-Drechsel Cyclization E. Drechsel, J. Prakt. Chem. 38(2), 69 (1858); W. Borsche, M. Feise, Ber. 20, 378 (1904). Formation of by acid-catalyzed r
  • Hunsdiecker Reaction
  • Hunsdiecker Reaction (Borodine Reaction) C. Hunsdiecker et al., US 2176181 (1939); H. Hunsdiecker, C. Hunsdiecker, Ber. 75, 291 (1942); A. Borodine, Ann. 119, 121 (1861).
  • Boord Olefin Synthesis
  • Boord Olefin Synthesis L. C. Swallen, C. E. Boord, J. Am. Chem. Soc. 52, 651 (1930); 53, 1505 (1931); 55, 3293 (1933); H. B. Dykstra et al., ibid. 52, 3396 (1930).
  • Bohn-Schmidt Reaction
  • Bohn-Schmidt Reaction R. Bohn, DE 46654 (1889); R. E. Schmidt, DE 60855 (1891). Hydroxylation of anthraquinones containing at least one hydroxyl group b
  • Bogert-Cook Synthesis
  • Bogert-Cook Synthesis M. T. Bogert, Science 77, 289 (1933); J. W. Cook, C. L. Hewett, J. Chem. Soc. 1933, 1098. Condensation of β-phenylethylmagnes
  • Bodroux-Chichibabin Aldehyde Synthesis
  • Bodroux-Chichibabin Aldehyde Synthesis F. Bodroux, Compt. Rend. 138, 92 (1904); A. E. Chichibabin, Ber. 37, 186, 850 (1904). Formation of aldehydes by t
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