Cyclization of 1,5-dinitrile systems with hydrogen halides: A search for the undetected key tautomer

Jordi Teixidó, José I. Borrell, Blanca Serra, Carles Colominas, Xavier Batllori, Joan F. Piniella, Angel Alvarez-Larena

Producción científica: Artículo en revista indizadaArtículorevisión exhaustiva

5 Citas (Scopus)

Resumen

The 13C NMR spectra of the pyridones 7a-d recorded in DMSO-d6 show three groups of signals which correspond to the two diastereomers of the 7-exo tautomer and the 7-endo tautomer. The X-ray powder analysis and the molecular structures of 7a-c clearly prove that these compounds, and probably 7d, are present in the solid state as a single diastereomer of the 7-exo tautomer which, on being dissolved, establishes an equilibrium with the other diastereomer through the 7-endo tautomer. This later had been proposed as a hey intermediate in the cyclization of the 1,5-dinitrile system present in 7a-d but was not previously detected.

Idioma originalInglés
Páginas (desde-hasta)4487-4496
Número de páginas10
PublicaciónTetrahedron
Volumen53
N.º12
DOI
EstadoPublicada - 24 mar 1997

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