Tandem Claisen rearrangement/Diels-Alder reaction in ionic liquid / 中国药科大学学报
Journal of China Pharmaceutical University
;
(6): 481-485, 2009.
Artigo
em Chinês
| WPRIM
| ID: wpr-480423
ABSTRACT
Aim:
The tandem Claisen rearrangement/Diels-Alder reaction in ionic liquid was carried out to find better changes for the conversion.Methods:
The synthesis started with replaced benzoic acid via acylation, cycli-zation, demethylation, allylation and then tandem Claisen rearrangement/Diels-Alder reaction in trational solvent and ionic liquid separately.Results:
BmimBF_4 raised the yield of the target compound and shortened the reaction time compared with the traditional solventConclusion:
BmimBF_4 can promote the tandem Claisen rearrange-ment/Diels-Alder reaction.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Idioma:
Chinês
Revista:
Journal of China Pharmaceutical University
Ano de publicação:
2009
Tipo de documento:
Artigo
Similares
MEDLINE
...
LILACS
LIS