Control de la quimioselectividad en la síntesis de heterociclos nitrogenados
- Pablo Peña Calleja 1
- María García Valverde 1
- Pablo Pertejo 1
- Roberto Quesada 1
-
1
Universidad de Burgos
info
- Joaquín Antonio Pacheco Bonrostro (dir.)
- José Luis Cuesta Gómez (coord.)
Publisher: Servicio de Publicaciones e Imagen Institucional ; Universidad de Burgos
ISBN: 978-84-16283-30-9, 84-16283-30-3
Year of publication: 2016
Pages: 299-303
Congress: Jornadas de Doctorandos de la Universidad de Burgos (3. 2016. Burgos)
Type: Conference paper
Abstract
Two families of nitrogen-based heterocycles, oxazolones and hydantoins, have been synthesized through a sequence Ugi/intramolecular ciclyzation. The chemoselectivity of the cyclization is governed by the nature of the major tautomer present in the Ugi adduct due to the employment of arylglioxals as starting materials.
Portal documents are updated daily. This date refers to the updating of information related to the portal structure (people, research groups, organizational units, projects...).