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  • An Improved and Mild Wenker Synthesis of Aziridines
    [作者:LI XINYAO; CHEN NING; XU JIAXI,期刊:Synthesis, 页码:3423-3428 , 文章类型: Article,,卷期:2010年-20]
  • The conventional Wenker synthesis of aziridines from vicinal amino alcohols has been modified by employing mild reaction conditions. Amino alcohols were converted into their hydrogen sulfates with chlorosulfonic acid. Th...
  • Novel Aromatic Fluoroolefins via Fluoro-Julia-Kocienski Olefination
    [作者:ALLENDOERFER NADINE; ESSAYED MAZEN; NIEGER MARTIN; BRAESE STEFAN,期刊:Synthesis, 页码:3439-3448 , 文章类型: Article,,卷期:2010年-20]
  • Fluoroolefins, which play an increasingly important role as peptide mimics in pharmaceuticals and as crop protection agents, are generated using a fluoro-Julia-Kocienski olefination. Their preparation can easily be accom...
  • An Efficient Total Synthesis of (+)-Varitriol from D-Ribonolactone
    [作者:KARLUBIKOVA OLGA; PALIK MIROSLAV; LASIKOVA ANGELIKA; GRACZA TIBOR,期刊:Synthesis, 页码:3449-3452 , 文章类型: Article,,卷期:2010年-20]
  • A short and efficient total synthesis of cytotoxic natural (+)-varitriol has been accomplished in eight steps from gamma-D-ribonolactone and 2,3-dimethylanisole in 41% overall yield. The key features include a highly ste...
  • Synthesis of Enantiopure Planar-Chiral Thiourea Derivatives
    [作者:SCHNEIDER JAKOB F; FROEHLICH ROLAND; PARADIES JAN,期刊:Synthesis, 页码:3486-3492 , 文章类型: Article,,卷期:2010年-20]
  • An efficient access to enantiopure pseudo-geminally substituted 4-amino-13-bromo[2.2]paracyclophane is described. The aminobromide was employed in cross-coupling reactions to yield arylated 4-amino[2.2]paracyclophanes. T...
  • Synthesis of (+)-Hanagokenol A, (+)-Fortunins E, G, H, and (-)-Sugikurojin A from Abietic Acid
    [作者:ALVAREZMANZANEDA ENRIQUE; CHAHBOUN RACHID; ALVAREZ ESTEBAN; RAMOS JOSE M; GUARDIA JUAN J; MESSOURI IBTISSAM; CHAYBOUN IKRAM; MANSOUR AHMED I; DAHDOUH ABDELAZIZ,期刊:Synthesis, 页码:3493-3503 , 文章类型: Article,,卷期:2010年-20]
  • A series of 12-hydroxy-substituted abietane diterpenes, functionalized on C19 or C18, have been synthesized starting from 18-hydroxyferruginol. The first synthesis of antibacterial hanagokenol A and fortunins E, G, and H...