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Epoxidation of allylic alcohols by hydrogen peroxide in the presence of complexed peroxotungstic species
- Source :
- Journal of Molecular Catalysis A: Chemical, Journal of Molecular Catalysis A: Chemical, Elsevier, 1996, 114, pp.77-85
- Publication Year :
- 1996
- Publisher :
- Elsevier BV, 1996.
-
Abstract
- Peroxotungstic acid and quaternary ammonium peroxotungstic salts when complexed to organophosphorus(V) ligands exhibit enhanced reactivity and selectivity in the epoxidation of unsaturated alcohols with hydrogen peroxide. The organophosphorus ligands contain the phosphoryl OP subunit as complexing moiety and are related to phosphine oxide, arylphosphonic acid and acidic phosphate ester. Allylic and cinnamic alcohols were examined under homogeneous and biphasic liquid-liquid conditions.
- Subjects :
- Phosphine oxide
Allylic rearrangement
010405 organic chemistry
Process Chemistry and Technology
[CHIM.CATA] Chemical Sciences/Catalysis
Alcohol
[CHIM.CATA]Chemical Sciences/Catalysis
010402 general chemistry
01 natural sciences
Catalysis
0104 chemical sciences
Amine oxide
chemistry.chemical_compound
chemistry
Polymer chemistry
Moiety
Organic chemistry
Reactivity (chemistry)
Physical and Theoretical Chemistry
Hydrogen peroxide
Subjects
Details
- ISSN :
- 13811169
- Volume :
- 114
- Database :
- OpenAIRE
- Journal :
- Journal of Molecular Catalysis A: Chemical
- Accession number :
- edsair.doi.dedup.....5cd515507e6bddd04a1e24bbf1a7c96d
- Full Text :
- https://doi.org/10.1016/s1381-1169(96)00305-6