A mild and convenient one-pot photochemical synthesis of chroman-4-one derivatives. the photo-Fries rearrangement of (hetero)aryl 3-methyl-2-butenoate esters under basic catalysis
The biphasic base catalysis-mediated photo-Fries rearrangement reaction of aryl 3-methy-2-butenoate esters in room temperature cyclohexane - 10% KOH system was investigated. This mild photochemical reaction leads to the formation of chroman-4-one derivatives in good to high yield and in short reacti...
Guardado en:
| Autores principales: | López, C.S., Erra-Balsells, R., Bonesi, S.M. |
|---|---|
| Formato: | JOUR |
| Materias: | |
| Acceso en línea: | http://hdl.handle.net/20.500.12110/paper_00404039_v51_n33_p4387_Lopez |
| Aporte de: |
Ejemplares similares
-
A mild and convenient one-pot photochemical synthesis of chroman-4-one derivatives. the photo-Fries rearrangement of (hetero)aryl 3-methyl-2-butenoate esters under basic catalysis
Publicado: (2010) -
Expeditious photochemical reaction toward the preparation of substituted chroman-4-ones
Publicado: (2014) -
Expeditious photochemical reaction toward the preparation of substituted chroman-4-ones
por: Iguchi, D., et al. -
Formation of 2,2-dimethylchroman-4-ones during the photoinduced rearrangement of some aryl 3-methyl-2-butenoate esters. A mechanistic insight
por: Erra Balsells, Rosa, et al.
Publicado: (2016) -
Formation of 2,2-dimethylchroman-4-ones during the photoinduced rearrangement of some aryl 3-methyl-2-butenoate esters. A mechanistic insight
por: Iguchi, D., et al.