A Convenient Procedure for Friedlander Synthesis of Quinoline Derivatives Catalyzed by Zirconium Dodecylphosphonate as an Efficient and Reusable Catalyst
نویسندگان: ثبت نشده
چکیده مقاله:
2-Amino-substituted ketones react with α-methylene ketones under solvent-free conditions at 90 °C in thepresence of a catalytic amount of zirconium dodecylphosphonate to create the corresponding quinolinesin excellent yields. This procedure recommends numerous advantages such as easy work-up, use of mild,reusable and safe catalyst, short reaction timeand high yields. The new compounds have been characterizedby 1H-NMR, 13C-NMR, mass and elemental analysis data.
منابع مشابه
a convenient procedure for friedlander synthesis of quinoline derivatives catalyzed by zirconium dodecylphosphonate as an efficient and reusable catalyst
2-amino-substituted ketones react with α-methylene ketones under solvent-free conditions at 90 °c in thepresence of a catalytic amount of zirconium dodecylphosphonate to create the corresponding quinolinesin excellent yields. this procedure recommends numerous advantages such as easy work-up, use of mild,reusable and safe catalyst, short reaction timeand high yields. the new compounds have been...
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In the present of methylimidazolium hydrogen sulfate, the synthesis of arylidene heterobicyclic pyrimidinones is studied by condensation of aromatic aldehyde, cyclopentanone, and urea or thiourea. Using solvent-free conditions, non-toxic and inexpensive materials, simple and clean work-up, short reaction times and good yields of the products are the advantages of this method.
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عنوان ژورنال
دوره 3 شماره 2
صفحات 195- 199
تاریخ انتشار 2015-08-01
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