Issue 11, 2011

A supported palladium nanocatalyst for copper free acyl Sonogashira reactions: One-pot multicomponent synthesis of N-containing heterocycles

Abstract

A convenient method has been developed for the synthesis of palladium nanoparticles (PdNPs) embedded into a polymer matrix, PPS [PPS = poly(1,4-phenylene sulfide)], via the thermolysis of palladium acetate. X-ray photoelectron spectroscopy (XPS) studies confirmed the presence of strong sulfur coordination of PPS to the palladium nanoclusters. These palladium nanoparticles (PdNPs-PPS) have been used as an efficient heterogeneous nanocatalytic system for the copper free acyl Sonogashira reaction. A wide range of ynones was synthesized in high yields under mild reaction conditions. The catalyst was recovered and recycled up to four times. Transmission electron microscopy (TEM) images revealed that the catalyst maintained nanospheric dimensions for four consecutive catalytic cycles. This simple protocol was further explored in a one-pot multicomponent synthesis of 2,4-disubstituted pyrimidines and a tetrahydro-β-carboline derivative in improved yield.

Graphical abstract: A supported palladium nanocatalyst for copper free acyl Sonogashira reactions: One-pot multicomponent synthesis of N-containing heterocycles

Supplementary files

Article information

Article type
Paper
Submitted
18 Jul 2011
Accepted
24 Aug 2011
First published
19 Sep 2011

Green Chem., 2011,13, 3238-3247

A supported palladium nanocatalyst for copper free acyl Sonogashira reactions: One-pot multicomponent synthesis of N-containing heterocycles

S. Santra, K. Dhara, P. Ranjan, P. Bera, J. Dash and S. K. Mandal, Green Chem., 2011, 13, 3238 DOI: 10.1039/C1GC15869D

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