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  • Bischler-Möhlau Indole Synthesis
  • Bischler-Möhlau Synthesis A. Bischler et al., Ber. 25, 2860 (1892); 26, 1336 (1893); R. Möhlau, ibid. 14, 171 (1881); 15, 2480 (1882); E. Fischer, T. Schmitt, i
  • Birch Reduction
  • Birch Reduction A. J. Birch, J. Chem. Soc. 1944, 430; 1945, 809; 1946, 593; 1947, 102, 1642, 1949, 2531. Reduction of aromatic rings by means of alkali
  • Biginelli Reaction
  • Biginelli Reaction P. Biginelli, Ber. 24, 1317, 2962 (1891); 26, 447 (1893). Synthesis of tetrahydropyrimidinones by the acid-catalyzed condensation of
  • Doebner-Miller Reaction
  • Doebner-Miller Reaction; Beyer Method for s O. Doebner, W. v. Miller, Ber. 16, 2464 (1883). Acid-catalyzed synthesis of quinolines from primary aromatic
  • Betti Reaction
  • Betti Reaction M. Betti, Gazz. Chim. Ital. 30 II, 301 (1900); 33 II, 2 (1903); F. Pirrone, ibid. 66, 518 (1936); 67, 529 (1937). The reaction of aromati
  • Bernthsen Acridine Synthesis
  • Bernthsen Synthesis A. Bernthsen, Ann. 192, 1 (1878); 224, 1 (1884). Formation of 5-substituted acridines by heating diarylamines in organic acids or a
  • Bucherer-Bergs Reaction
  • Bucherer-Bergs Reaction H. T. Bucherer, H. T. Fischbeck, J. Prakt. Chem. 140, 69 (1934); H. T. Bucherer, W. Steiner, ibid. 291; H. Bergs, DE 566094 (1929).
  • Bergmann-Zervas Carbobenzoxy Method
  • Bergmann-Zervas Carbobenzoxy Method M. Bergmann, L. Zervas, Ber. 65, 1192 (1932). Formation of the N-carbobenzoxy derivative of an amino acid for use in
  • Bergmann Degradation
  • Bergmann Degradation M. Bergmann, Science 79, 439 (1934). Stepwise degradation of polypeptides involving benzoylation, conversion to azides and treatmen
  • Bergmann Azlactone Peptide Synthesis
  • Bergmann Azlactone Peptide Synthesis M. Bergmann et al., Ann. 449, 277 (1926). Conversion of an acetylated amino acid and an aldehyde into an azlactone
  • Bergman Reaction
  • Bergman Reaction R. R. Jones, R. G. Bergman, J. Am. Chem. Soc. 94, 660 (1972); R. G. Bergman, Accts. Chem. Res. 6, 25 (1973). The cyclization of enediyn
  • Bergius Process
  • Bergius Process F. Bergius, Gas World 58, 490 (1913); GB 18232 (1914). Formation of petroleum-like hydrocarbons by hydrogenation of coal at high tempera
  • Benzoin Condensation
  • Condensation A. J. Lapworth, J. Chem. Soc. 83, 995 (1903); 85, 1206 (1904). -catalyzed condensation of aromatic aldehydes to give benzoins (acyloins):
  • 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
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