A Convenient Procedure for Friedlander Synthesis of Quinoline Derivatives
Catalyzed by Zirconium Dodecylphosphonate as an Efficient and Reusable Catalyst
Document Type : Research Paper
Abstract
2-Amino-substituted ketones react with α-methylene ketones under solvent-free conditions at 90 °C in the presence of a catalytic amount of zirconium dodecylphosphonate to create the corresponding quinolines in 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 characterized by 1H-NMR, 13C-NMR, mass and elemental analysis data.
(2015). A Convenient Procedure for Friedlander Synthesis of Quinoline Derivatives
Catalyzed by Zirconium Dodecylphosphonate as an Efficient and Reusable Catalyst. Journal of Physical Chemistry & Eleectrochemistry, 3(2), 195-199.
MLA
. "A Convenient Procedure for Friedlander Synthesis of Quinoline Derivatives
Catalyzed by Zirconium Dodecylphosphonate as an Efficient and Reusable Catalyst". Journal of Physical Chemistry & Eleectrochemistry, 3, 2, 2015, 195-199.
HARVARD
(2015). 'A Convenient Procedure for Friedlander Synthesis of Quinoline Derivatives
Catalyzed by Zirconium Dodecylphosphonate as an Efficient and Reusable Catalyst', Journal of Physical Chemistry & Eleectrochemistry, 3(2), pp. 195-199.
VANCOUVER
A Convenient Procedure for Friedlander Synthesis of Quinoline Derivatives
Catalyzed by Zirconium Dodecylphosphonate as an Efficient and Reusable Catalyst. Journal of Physical Chemistry & Eleectrochemistry, 2015; 3(2): 195-199.
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