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.
引用
收藏
页码:4444 / 4450
页数:7
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