Oxidation of alkenes by oxodiperoxomolybdenum: Trialkyl(aryl)phosphine oxide complexes
被引:10
作者:
Kiraz, Christine I. Altinis
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h-index: 0
机构:
Rutgers State Univ, Dept Chem & Biol Chem, Piscataway, NJ 08854 USARutgers State Univ, Dept Chem & Biol Chem, Piscataway, NJ 08854 USA
Kiraz, Christine I. Altinis
[1
]
Mora, Luis
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h-index: 0
机构:
Rutgers State Univ, Dept Chem & Biol Chem, Piscataway, NJ 08854 USARutgers State Univ, Dept Chem & Biol Chem, Piscataway, NJ 08854 USA
Mora, Luis
[1
]
Jimenez, Leslie S.
论文数: 0引用数: 0
h-index: 0
机构:
Rutgers State Univ, Dept Chem & Biol Chem, Piscataway, NJ 08854 USARutgers State Univ, Dept Chem & Biol Chem, Piscataway, NJ 08854 USA
Jimenez, Leslie S.
[1
]
机构:
[1] Rutgers State Univ, Dept Chem & Biol Chem, Piscataway, NJ 08854 USA
来源:
SYNTHESIS-STUTTGART
|
2007年
/
01期
关键词:
epoxidations;
organometallic reagents;
heterogenous catalysis;
molybdenum complexes;
green chemistry;
D O I:
10.1055/s-2006-958933
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
Catalytic amounts of short-chain (2-4 carbons) trialkylphosphine oxide ligands and MoO5 have been shown to efficiently convert di- and higher substituted alkenes to the corresponding epoxides using a biphasic system with either 30% hydrogen peroxide or 70% TBHP acting as the stoichiometric oxidant.