Montmorillonite K-10 promoted synthesis of chiral dioxa-caged compounds derived from levoglucosenone.
Carbohydr Res
; 402: 67-70, 2015 Jan 30.
Article
em En
| MEDLINE
| ID: mdl-25497334
ABSTRACT
A short and efficient methodology for the synthesis of chiral dioxa-caged compounds from levoglucosenone, a biomass-derived enone, is herein presented. The key transformation, that involves a cascade 3-step cationic cyclization, was efficiently carried out in high yields and selectivities by Montmorillonite K-10 catalysis. The usefulness of K-10 in related semi-pinacol rearrangements to obtain pyran-3-ones is also shown. Interesting differences in the reactivity pattern was found for epimeric alcohols, and the origins of these findings were determined by DFT calculations.
Palavras-chave
Texto completo:
1
Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Bentonita
/
Compostos Bicíclicos Heterocíclicos com Pontes
/
Glucose
Tipo de estudo:
Prognostic_studies
Idioma:
En
Revista:
Carbohydr Res
Ano de publicação:
2015
Tipo de documento:
Article
País de afiliação:
Argentina