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  • Catalytic performance of zeolites H-BEA, H-MFI, H-FAU and H-MOR, exhibiting textural differences and with different Bronsted and Lewis acid sites concentration, have been studied in the synthesis of quinolines via Friedlander reaction. H-BEA and H-FAU efficiently promoted the condensation of 2-aminoaryl ketones 3 with ethyl acetoacetate (4a) or acetylacetone (4b) under mild reaction conditions, those being the first examples of zeolites as catalysts for this transformation. While H-FAU showed similar catalytic behaviour than that reported for (Al)SBA-15 affording mixtures of quinolines 5 and quinolones 6, H-BEA mainly led to quinolines 5 in almost total selectivity and good yields. However, H-MFI and H-MOR zeolites afforded quinolones 6 as the major reaction product. Methodology reported here was found to be useful for the synthesis of biologically active compounds with excellent yields avoiding unnecessary purifications protocols and tedious work-up procedures.
  • Catalytic performance of zeolites H-BEA, H-MFI, H-FAU and H-MOR, exhibiting textural differences and with different Bronsted and Lewis acid sites concentration, have been studied in the synthesis of quinolines via Friedlander reaction. H-BEA and H-FAU efficiently promoted the condensation of 2-aminoaryl ketones 3 with ethyl acetoacetate (4a) or acetylacetone (4b) under mild reaction conditions, those being the first examples of zeolites as catalysts for this transformation. While H-FAU showed similar catalytic behaviour than that reported for (Al)SBA-15 affording mixtures of quinolines 5 and quinolones 6, H-BEA mainly led to quinolines 5 in almost total selectivity and good yields. However, H-MFI and H-MOR zeolites afforded quinolones 6 as the major reaction product. Methodology reported here was found to be useful for the synthesis of biologically active compounds with excellent yields avoiding unnecessary purifications protocols and tedious work-up procedures. (en)
Title
  • Zeolites Promoting Quinoline Synthesis via Friedlander Reaction
  • Zeolites Promoting Quinoline Synthesis via Friedlander Reaction (en)
skos:prefLabel
  • Zeolites Promoting Quinoline Synthesis via Friedlander Reaction
  • Zeolites Promoting Quinoline Synthesis via Friedlander Reaction (en)
skos:notation
  • RIV/61388955:_____/10:00437032!RIV15-GA0-61388955
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • P(GD203/08/H032), Z(AV0Z40400503)
http://linked.open...iv/cisloPeriodika
  • 19-20
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
http://linked.open.../riv/druhVysledku
http://linked.open...iv/duvernostUdaju
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  • 299927
http://linked.open...ai/riv/idVysledku
  • RIV/61388955:_____/10:00437032
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • heterogeneous catalysis; zeolites; quinolines (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • NL - Nizozemsko
http://linked.open...ontrolniKodProRIV
  • [342B9B71B549]
http://linked.open...i/riv/nazevZdroje
  • Topics in Catalysis
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...vavai/riv/projekt
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 53
http://linked.open...iv/tvurceVysledku
  • Pérez-Mayoral, E.
  • Vitvarová, Dana
  • López-Peinado, A. J.
  • Martín-Aranda, R. M.
  • López-Sanz, J.
http://linked.open...ain/vavai/riv/wos
  • 000283584800019
http://linked.open...n/vavai/riv/zamer
issn
  • 1022-5528
number of pages
http://bibframe.org/vocab/doi
  • 10.1007/s11244-010-9603-8
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