Elbs Reaction K. Elbs, E. Larsen, Ber. 17, 2847 (1884). Formation of polyaromatics (eg. anthracene) by intramolecular condensation of diaryl ketones con
Elbs Persulfate Oxidation K. Elbs, J. Prakt. Chem. 48, 179 (1893). Hydroxylation of monophenols to predominantely p-diphenols or oxidation of methyl-sub
Tscherniac-Einhorn Reaction J. Tscherniac, DE 134979; A. Einhorn et al., Ann. 343, 207 (1905); 361, 113 (1908). Introduction of the amidomethyl group in
Ehrlich-Sachs Reaction P. Ehrlich, F. Sachs, Ber. 32, 2341 (1899). Formation of N-phenylimines by the base-catalyzed condensation of compounds containin
Edman Degradation P. Edman, Acta Chem. Scand. 4, 283 (1950). Cyclic degradation of peptides based on the reaction of phenylisothiocyanate with the free
Eastwood Reaction (Eastwood Deoxygenation) G. Grank, F. W. Eastwood, Aust. J. Chem. 17, 1392 (1964). Stereospecific conversion of vicinal diols into ole
Dutt-Wormall Reaction P. K. Dutt, H. R. Whitehead, A. Wormall, J. Chem. Soc. 119, 2088 (1921); P. K. Dutt, ibid. 125, 1463 (1924). Preparation of diazoa
Frankland-Duppa Reaction E. Frankland, Ann. 126, 109 (1863); E. Frankland, B. F. Duppa, Ann. 135, 25 (1865). Formation of α-hydroxycarboxylic este
Duff Reaction J. C. Duff, E. J. Bills, J. Chem. Soc. 1932, 1987; 1934, 1305; 1941, 547; 1945, 276. Formylation of phenols or aromatic amines with hexame
Dötz Reaction K. H. Dötz, Angew. Chem. Int. Ed. 14, 644 (1975). Three component cyclization of an aromatic or vinylic alkoxy pentacarbonyl chr
Doering-LaFlamme Allene Synthesis W. von E. Doering, P. M. LaFlamme, Tetrahedron 2, 75 (1958); US 2933544 (1960). Treatment of an olefin with bromoform
Doebner Reaction O. Doebner, Ann. 242, 265 (1887); Ber. 20, 277 (1887); 27, 352, 2020 (1894). Formation of substituted cinchoninic acids from aromatic a
Knoevenagel Condensation; Doebner Modification E. Knoevenagel Ber. 31, 2596 (1898); O. Doebner, Ber. 33, 2140 (1900). Condensation of aldehydes or keton
Dimroth Rearrangement O. Dimroth, Ann. 364, 183 (1909); 459, 39 (1927). Rearrangement whereby exo- and endocyclic heteroatoms on a heterocyclic ring are
Dienone- Rearrangement K. von Auwers, K. Ziegler, Ann. 425, 217 (1921). Transformation of a 4,4-disubstituted cyclohexadienone into a 3,4-disubstituted
Dieckmann Reaction W. Dieckmann, Ber. 27, 102, 965 (1894); 33, 595, 2670, (1900); Ann. 317, 51, 93, (1901). Base-catalyzed cyclization of dicarboxylic a
Dess-Martin Oxidation D. B. Dess, J. C. Martin, J. Org. Chem. 48, 4155 (1983). Mild oxidation of primary and secondary alcohols to aldehydes and ketones
Demjanov Rearrangement N. J. Demjanov, M. Lushnikov, J. Russ. Phys. Chem. Soc. 35, 26 (1903); Chem. Zentr. 1903, 1, 828. Deamination of primary amines b
Tiffeneau-Demjanov Rearrangement M. Tiffeneau et al., Compt. Rend. 205, 54 (1937). Rearrangement of β-amino alcohols upon diazotization with nitrou
Delépine Reaction (Delépine Amine Synthesis) M. Delépine, Compt. Rend. 120, 501 (1895); 124, 292 (1897). Preparation of primary ami
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