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  • Stereocontrol Strategies in the Asymmetric Bioreduction of Alkenes
    [作者:OBERDORFER GUSTAV; GRUBER KARL; FABER KURT; HALL MELANIE,期刊:SYNLETT, 页码:1857-1864 , 文章类型: Article,,卷期:2012年-13]
  • The asymmetric bioreduction of prochiral conjugated alkenes using ene-reductases allows powerful strategies to access both enantiomers of the product with high stereoselectivity. This may be achieved (i) by using pairs o...
  • Asymmetric Cyanation with the Chiral Ru-Li Combined Catalysts
    [作者:OHKUMA TAKESHI; KURONO NOBUHITO,期刊:SYNLETT, 页码:1865-1881 , 文章类型: Article,,卷期:2012年-13]
  • The combined systems of phenylglycinate/BINAP/Ru(II) complex and Li compounds have been found to act as highly reactive and enantioselective catalysts for cyanosilylation and hydrocyanation of aldehydes, alpha-keto ester...
  • Novel One-Pot Synthesis of Thiophenols from Related Triazenes under Mild Conditions
    [作者:KHAZAEI ARDESHIR; KAZEMROSTAMI MASOUD; MOOSAVIZARE AHMAD REZA; BAYAT MOHAMMAD; SAEDNIA SHAHNAZ,期刊:SYNLETT, 页码:1893-1896 , 文章类型: Article,,卷期:2012年-13]
  • In this work, at first, triazenes were synthesized from primary aryl amines. Afterwards, triazenes were converted into the corresponding thiophenols in one-pot using sodium sulfide in acidic media, by in situ generation ...
  • [3+2] Cycloaddition of Masked o-Benzoquinones with Azomethine Ylides
    [作者:CHITTIMALLA SANTHOSH KUMAR; KUPPUSAMY RAJESH; CHAKRABARTI ANJAN,期刊:SYNLETT, 页码:1901-1906 , 文章类型: Article,,卷期:2012年-13]
  • A simple and efficient access to highly functionalized isoindolone derivatives via a [3+2] cycloaddition process between in situ generated azomethine ylides with various stable (isolable) masked o-benzoquinones is descri...
  • General Synthetic Approach to 2-Phenolic Adenine Derivatives
    [作者:CORREIA CARLA; ALICE CARVALHO M; ROCHA ASHLY; FERNANDA PROENCA M,期刊:SYNLETT, 页码:1923-1926 , 文章类型: Article,,卷期:2012年-13]
  • A simple and general 'one-pot' procedure for the synthesis of 2,9-diarylpurines with one or multiple hydroxyl groups in the 2-aryl unit is described, from the reaction of 5-amino-4-amidinoimidazoles with phenolic aldehyd...