Saltar al contenido
Merck

Spirocyclic dihydropyridines by electrophile-induced dearomatizing cyclization of N-alkenyl pyridinecarboxamides.

Organic letters (2013-04-04)
Jemma Senczyszyn, Heloise Brice, Jonathan Clayden
RESUMEN

On treatment with acylating or sulfonylating agents, N-alkenyl pyridine carboxamides (N-pyridinecarbonyl enamines) undergo a dearomatizing cyclization initiated by pyridine acylation and followed by intramolecular trapping of the resulting pyridinium cation. The products are spirocyclic dihydropyridines which may be further elaborated to spirocyclic heterocycles with drug-like features.

MATERIALES
Referencia del producto
Marca
Descripción del producto

Sigma-Aldrich
Isonicotinamide, ReagentPlus®, 99%