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  • Formal Total Synthesis of (-)-5,6-Dihydrocineromycine B
    [作者:REDDY G VENKATESWAR; KUMAR R SATEESH CHANDRA; SIVA B; BABU K SURESH; RAO J MADHUSUDANA,期刊:SYNLETT, 页码:2677-2681 , 文章类型: Article,,卷期:2012年-18]
  • An efficient and highly convergent formal total synthesis of the 14-membered macrolide (-)-5,6-dihydrocineromycine B is achieved. Key reaction sequences include a Sharpless asymmetric epoxidation followed by esterificati...
  • New Simple Synthesis of Quinoline-4-carbonitriles
    [作者:BUJOK ROBERT; TRAWCZYNSKI ADAM; WROBEL ZBIGNIEW; WOJCIECHOWSKI KRZYSZTOF,期刊:SYNLETT, 页码:2682-2686 , 文章类型: Article,,卷期:2012年-18]
  • Alkylation of 2-nitrobenzyl cyanides with alpha-halomethyl ketones furnishes ketonitriles which upon reduction with tin(II) chloride form quinoline-4-carbonitriles in good yields.
  • PEG 400
    [作者:SINGH UDAYA PRATAP,期刊:SYNLETT, 页码:2721-2722 , 文章类型: Editorial Material,,卷期:2012年-18]
  • Biomimetic Syntheses of the Flindersial Alkaloids
    [作者:VALLAKATI RAVIKRISHNA; MAY JEREMY A,期刊:SYNLETT, 页码:2577-2581 , 文章类型: Article,,卷期:2012年-18]
  • The flindersial alkaloids have a potentially novel mechanism for antimalarial activity. The recently disclosed flinderoles were postulated to be derived through dimerization of the natural product borrerine in a manner s...
  • Garrat t-Braverman Cyclization, a Powerful Tool for C-C Bond Formation
    [作者:MONDAL SAYANTAN; MITRA TAPOBRATA; MUKHERJEE RAJA; ADDY PARTHA SARATHI; BASAK AMIT,期刊:SYNLETT, 页码:2582-2602 , 文章类型: Article,,卷期:2012年-18]
  • Development of new strategies for C-C bond formation remains in the forefront of organic synthesis. The base-mediated rearrangement of bis-propargyl sulfones via bis-allenes generated in situ, now known as the Garratt-Br...
  • Transition-Metal-Catalyzed Arylation of 1-Deazapurines via C-H Bond Activation
    [作者:IAROSHENKO VIKTOR O; ALI IFTIKHAR; MKRTCHYAN SATENIK; SEMENIUCHENKO VOLODYMYR; OSTROVSKYI DMYTRO; LANGER PETER,期刊:SYNLETT, 页码:2603-2608 , 文章类型: Article,,卷期:2012年-18]
  • Transition-metal-catalyzed arylation of imidazo[4,5-b] pyridines (known as 1-deazapurines) is reported. 1-Deazapurines were synthesized from 5-aminoimidazoles, generated in situ by the reaction of methyl N-(cyanomethyl)f...