4.4 Article

Transition-Metal-Catalyzed Arylation of 1-Deazapurines via C-H Bond Activation

Journal

SYNLETT
Volume -, Issue 18, Pages 2603-2608

Publisher

GEORG THIEME VERLAG KG
DOI: 10.1055/s-0032-1317329

Keywords

catalysis; nickel; C-H activation; arylation; 1-deazapurine; imidazole

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Transition-metal-catalyzed arylation of imidazo[4,5-b] pyridines (known as 1-deazapurines) is reported. 1-Deazapurines were synthesized from 5-aminoimidazoles, generated in situ by the reaction of methyl N-(cyanomethyl)formimidate with primary amines.

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