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Manganese catalyzed cis-dihydroxylation of electron deficient alkenes with H2O2
被引:38
|作者:
Saisaha, Pattama
[1
]
Pijper, Dirk
[1
]
van Summeren, Ruben P.
[2
]
Hoen, Rob
[1
]
Smit, Christian
[1
]
de Boer, Johannes W.
[3
]
Hage, Ronald
[3
]
Alsters, Paul L.
[2
]
Feringa, Ben L.
[1
]
Browne, Wesley R.
[1
]
机构:
[1] Univ Groningen, Fac Math & Nat Sci, Stratingh Inst Chem, NL-9747 AG Groningen, Netherlands
[2] DSM Innovat Synth, NL-6160 MD Geleen, Netherlands
[3] Rahu Catalyt BV, BioPartner Ctr Leiden, NL-2333 AL Leiden, Netherlands
关键词:
HYDROGEN-PEROXIDE;
EPOXIDATION;
OXIDATION;
OLEFINS;
SYSTEM;
ACID;
COMPLEXES;
ALCOHOLS;
D O I:
10.1039/c0ob00102c
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
A practical method for the multigram scale selective cis-dihydroxylation of electron deficient alkenes such as diethyl fumarate and N-alkyl and N-aryl-maleimides using H2O2 is described. High turnovers (> 1000) can be achieved with this efficient manganese based catalyst system, prepared in situ from a manganese salt, pyridine-2-carboxylic acid, a ketone and a base, under ambient conditions. Under optimized conditions, for diethyl fumarate at least 1000 turnovers could be achieved with only 1.5 equiv. of H2O2 with d/l-diethyl tartrate (cis-diol product) as the sole product. For electron rich alkenes, such as cis-cyclooctene, this catalyst provides for efficient epoxidation.
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页码:4444 / 4450
页数:7
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