Selective Catalytic Isomerization of ß-Pinene Oxide to Perillyl Alcohol Enhanced by Protic Tetraimidazolium Nitrate.
ChemistryOpen
; 10(4): 477-485, 2021 04.
Article
en En
| MEDLINE
| ID: mdl-33908700
A series of tetraimidazolium salts with different anions was prepared and applied in the isomerization of ß-pinene oxide. After examining the activity of different catalysts, a remarkable enhancement of the selectivity of perillyl alcohol (47 %) was obtained over [PEimi][HNO3 ]4 under mild reaction conditions and using DMSO as the solvent. Furthermore, noncovalent interactions between solvent molecules and the catalyst were found by FT-IR spectroscopy and confirmed by computational chemistry. The homogeneous catalyst showed excellent stability and was reused up to six times without significant loss.
Texto completo:
1
Colección:
01-internacional
Base de datos:
MEDLINE
Idioma:
En
Revista:
ChemistryOpen
Año:
2021
Tipo del documento:
Article
País de afiliación:
China
Pais de publicación:
Alemania