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  • Regiospecific bromination of 2-phenyl-3H-pyrimidin-4-ones.
    [作者:Zanatta, Nilo;Fantinel, Leonardo;Fernandes, Liana da S.;Wouters, Ana D.;Bonacorso, Helio G.;Martins, Marcos A. P.;,期刊:Synthesis, 页码:3492-3496 , 文章类型: 研究论文,,卷期:2008年-21]
  • Three methods for the regiospecific bromination of 2-phenyl-3H-pyrimidin-4-ones are presented: bromination of the 5-position of the pyrimidine ring, bromination of the 6-benzylic position, and simultaneous bromination of...
  • An improved preparation of 3-alkoxypyrazoles.
    [作者:Guillou, Sandrine;Bonhomme, Frederic J.;Janin, Yves L.;,期刊:Synthesis, 页码:3504-3508 , 文章类型: 研究论文,,卷期:2008年-21]
  • The condensation between alkyl acetoacetates and hydrazines constitutes the very well-known Knorr synthetic method leading to pyrazol-3/5-ones. However, contemporary reports describe an alternate reaction pathway leadin...
  • Syntheses of aromatic substituted 6'-thiothalidomides.
    [作者:Luo, Weiming;Yu, Qian-sheng;Tweedie, David;Deschamps, Jeffery;Parrish, Damon;Holloway, Harold W.;Li, Yazhou;Brossi, Arnold;Greig, Nigel H.;,期刊:Synthesis, 页码:3415-3422 , 文章类型: 研究论文,,卷期:2008年-21]
  • A resurgence of interest in thalidomide has occurred as a consequence of its diverse immunomodulatory and anticancer actions, which has fueled interest in synthetic analogs with higher potencies or less undesirable side ...
  • Preparation of dicyano- and methylcobinamide from vitamin B12a.
    [作者:Wedemeyer-Exl, Christina;Darbre, Tamis;Keese, Reinhart;,期刊:Synthesis, 页码:3429-3432 , 文章类型: 研究论文,,卷期:2008年-21]
  • Treatment of vitamin B12a (hydroxycobalamin HCl, aquocobalamin) with NaBH4 and ZnCl2 leads to the selective cleavage of the nucleotide loop and gives dicyanocobinamide in good yield. Methylcobinamide was prepd. from the...
  • Extension of the library of biologically active g-alkylidene butenolides.
    [作者:Novak, Petr;Pour, Milan;Spulak, Marcel;Votruba, Ivan;Kotora, Martin;,期刊:Synthesis, 页码:3465-3472 , 文章类型: 研究论文,,卷期:2008年-21]
  • g-Alkylidene butenolides bearing a deoxyriboside, a steroid, and a ferrocene moiety were synthesized by stereoselective sequential cross-coupling lactonization from appropriate terminal alkynes with 3-iodopropenoates. T...