INFIQC   05475
INSTITUTO DE INVESTIGACIONES EN FISICO- QUIMICA DE CORDOBA
Unidad Ejecutora - UE
artículos
Título:
Reactivity of endo-3-bromocamphor with sulfur-centered nucleophiles by an
Autor/es:
JORGE G. URANGA; ANA N SANTIAGO
Revista:
ORGANIC & BIOMOLECULAR CHEMISTRY
Editorial:
ROYAL SOC CHEMISTRY
Referencias:
Año: 2011 vol. 9 p. 2969 - 2974
ISSN:
1477-0520
Resumen:
The photostimulated reaction of arylthiolate ions with endo-3-bromocamphor produced both reduction and substitution products. The pKa and proton affinities of the conjugated acids were found to be good indicators of the reactivity.