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  • Benzilic Acid Rearrangement
  • Benzilic Acid Rearrangement (Benzil-Benzilic Acid Rearrangement) J. Liebig, Ann. 25, 27 (1838); N. Zinin, ibid. 31, 329 (1939). Base-induced rearrangeme
  • Benzidine Rearrangement
  • Benzidine Rearrangement; Semidine Rearrangement A. W. Hofmann, Proc. Roy. Soc. London 12, 576 (1863); P. Jacobson et al., Ber. 26, 688 (1893). Acid-cata
  • Benkeser Reduction
  • Benkeser Reduction R. A. Benkeser et al., J. Am. Chem. Soc. 74, 5699 (1952); 77, 3230 (1955). Reduction of aromatic and olefinic compounds with lithium
  • Bénary Reaction
  • Bénary Reaction E. Bénary, Ber. 63, 1573 (1930); 64, 2543 (1931). Action of Grignard reagents on enamino ketones or aldehydes yields &beta
  • Feist-Bénary Synthesis
  • Feist-Bénary Synthesis F. Feist, Ber. 35, 1537, 1545 (1902); E. Bénary, Ber. 44, 489, 493 (1911). Formation of furans from α-halogen
  • Fujimoto-Belleau Reaction
  • Fujimoto-Belleau Reaction C. I. Fujimoto, J. Am. Chem. Soc. 73, 1856 (1951); B. Belleau, ibid. 5441. Synthesis of cyclic α-substituted α,&be
  • Dowd-Beckwith Ring Expansion Reaction
  • Dowd-Beckwith Ring Expansion Reaction A. L. J. Beckwith et al., J. Am. Chem. Soc. 110, 2565 (1988); P. Dowd, S. C. Choi, Tetrahedron 45, 77 (1989). Free
  • Beckmann Rearrangement
  • Beckmann Rearrangement; Beckmann Fragmentation E. Beckmann, Ber. 19, 988 (1886). Acid-mediated isomerization of oximes to amides. Oximes of cyclic keton
  • Béchamp Reduction
  • Béchamp Reduction A. J. Béchamp, Ann. Chim. Phys. 42(3), 186, (1854). Reduction of aromatic nitro compounds to the corresponding amines by
  • Baylis-Hillman Reaction
  • Baylis-Hillman Reaction A. B. Baylis, M. E. D. Hillman, DE 2155113; eidem, US 3743669 (1972, 1973 both to Celanese). Coupling of activated vinyl systems
  • Schotten-Baumann Reaction
  • Schotten-Baumann Reaction C. Schotten, Ber. 17, 2544 (1884); E. Baumann, ibid. 19, 3218 (1886). Acylation of alcohols or amines with acid chlorides in a
  • Haller-Bauer Reaction
  • Haller-Bauer Reaction A. Haller, E. Bauer, Compt. Rend. 148, 70, 127 (1909); 149, 5 (1909). Cleavage of non-enolizable ketones with sodium amide; freque
  • Baudisch Reaction
  • Baudisch Reaction O. Baudisch et al., Naturwiss. 27, 768, 769 (1939); Science 92, 336 (1940); J. Am. Chem. Soc. 63, 622 (1941). Synthesis of o-nitrosoph
  • Barton-Zard Reaction
  • Barton-Zard Reaction D. H. R. Barton et al., Tetrahedron 46, 7587 (1990). Formation of a pyrrole by condensation of a substituted nitroso-alkene with an
  • Barton Reaction
  • Barton Reaction D. H. R. Barton et al., J. Am. Chem. Soc. 82, 2640 (1960); 83, 4076 (1961). Conversion of a nitrite ester to a γ-oximino alcohol b
  • Barton Olefin Synthesis
  • Barton Olefin Synthesis (Barton-Kellogg Reaction) D. H. R. Barton et al., Chem. Commun. 1970, 1226; R. M. Kellogg, S. Wassenaar, Tetrahedron Letters 1970, 1987; R. M. Kell
  • Barton Deoxygenation
  • Barton Deoxygenation (Barton-McCombie Reaction) D. H. R. Barton, S. W. McCombie, Perkin Trans. I 1975, 1574. Deoxygenation of alcohols via their thiocar
  • Barton Decarboxylation
  • Barton Decarboxylation D. H. R. Barton et al., Chem. Commun. 1983, 939; eidem, Tetrahedron 41, 3901 (1985). Radical decarboxylation of organic acids to
  • Bart Reaction
  • Bart Reaction; Scheller Modification H. Bart, DE 250264 (1910); DE 254092 (1910); DE 264924 (1910); DE 268172 (1912); Ann. 429, 55 (1922); E. Scheller, GB 261026; A. W. Ru
  • Barbier-Wieland Degradation
  • Barbier-Wieland Degradation H. Wieland, Ber. 45, 484 (1912); P. Barbier, R. Locquin, Compt. Rend. 156, 1443 (1913). Stepwise carboxylic acid degradation
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