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Chemical Reaction - Basic Chemical -

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  • 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
  • Bodroux Reaction
  • Bodroux Reaction F. Bodroux, Bull. Soc. Chim. France 33, 831 (1905), 35, 519 (1906); 1, 912 (1907); Compt. Rend. 138, 1427 (1904); 140, 1108 (1905); 142, 401 (1906).
  • Blanc Reaction-Blanc Rule
  • Blanc Reaction-Blanc Rule H. G. Blanc, Compt. Rend. 144, 1356 (1907). Cyclization of dicarboxylic acids on heating with acetic anhydride to give either
  • Blanc Reaction
  • Blanc Reaction (Chloromethylation) G. Blanc, Bull. Soc. Chim. France [4], 33, 313 (1923). Introduction of the chloromethyl group into aromatic rings on
  • Bouveault-Blanc Reduction
  • Bouveault-Blanc Reduction L. Bouveault, G. Blanc, Compt. Rend. 136, 1676 (1903); Bull. Soc. Chim. France [3] 31, 666 (1904). Formation of alcohols by re
  • Blaise Reaction
  • Blaise Reaction E. E. Blaise, Compt. Rend. 132, 478 (1901). Formation of β-oxoesters by treatment of α-bromocarboxylic esters with zinc in th
  • Blaise Ketone Synthesis
  • Blaise Ketone Synthesis; Blaise-Maire Reaction E. E. Blaise, A. Koehler, Bull. Soc. Chim. [4] 7, 215 (1910); E. E. Blaise, M. Maire, Compt. Rend. 145, 73 (1907); E. E. Bla
  • Bischler-Napieralski Reaction
  • Bischler-Napieralski Reaction A. Bischler, B. Napieralski, Ber. 26, 1903 (1893). Cyclodehydration of β-phenethylamides to 3,4-dihydro derivatives b
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