Journal
RSC ADVANCES
Volume 7, Issue 14, Pages 8323-8331Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c6ra28299g
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Funding
- CSIR, New Delhi
- DST, NewDelhi
- DAE, Government of India
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An efficient route for the synthesis of penta-substituted/functionalized-3,4-diarylated pyridines, biologically important templates, via pyridine C3-arylation of nicotinic acids has been developed. The poly-substituted nicotinic acid precursors were prepared by an established multicomponent condensation approach. This route shows an excellent opportunity for introducing versatile (hetero)aryls and other substituents/functionalities into the pyridine ring. Several of the synthesized compounds exhibited significant anti-proliferative properties.
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