Ligand-free Cu2O-catalyzed cross coupling of nitrogen heterocycles with iodopyridines

A practical and efficient strategy has been developed for the cross coupling of nitrogen heterocycles with halopyridines using ligand-free Cu2O as catalyst and Cs2CO3 as the base. The protocol is applicable to a series of highly functionalised heterocycles, such as 7-azaindole, indazole, indole, imi...

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Veröffentlicht in:Tetrahedron 2013-09, Vol.69 (35), p.7279-7284
Hauptverfasser: Teo, Yong-Chua, Yong, Fui-Fong, Sim, Shirlyn
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container_end_page 7284
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container_title Tetrahedron
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creator Teo, Yong-Chua
Yong, Fui-Fong
Sim, Shirlyn
description A practical and efficient strategy has been developed for the cross coupling of nitrogen heterocycles with halopyridines using ligand-free Cu2O as catalyst and Cs2CO3 as the base. The protocol is applicable to a series of highly functionalised heterocycles, such as 7-azaindole, indazole, indole, imidazole, pyrrole and pyrazole, affording the N-heteroaryl derivatives in high yields (up to 96%). [Display omitted]
doi_str_mv 10.1016/j.tet.2013.06.095
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source ScienceDirect Journals (5 years ago - present)
subjects CATALYSTS
COPPER OXIDE
Copper-catalyzed
Cross coupling
CUPROUS OXIDE
Derivatives
Imidazole
Iodopyridines
LIGANDS
N-Heteroarylation
NITROGEN
Nitrogen heterocyles
Pyrazole
Pyrroles
Strategy
Tetrahedrons
title Ligand-free Cu2O-catalyzed cross coupling of nitrogen heterocycles with iodopyridines
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