Source:http://linkedlifedata.com/resource/pubmed/id/21694667
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
6
|
| pubmed:dateCreated |
2011-6-22
|
| pubmed:abstractText |
Lithium diphenylbinaphtholate catalyzed the enantioselective Evans-Tishchenko reduction of achiral ?-hydroxyketones to afford monoacyl-protected 1,3-diols with high stereoselectivities. In the reaction of racemic ?-hydroxyketones, kinetic optical resolution occurred in a highly stereoselective manner.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:issn |
1420-3049
|
| pubmed:author | |
| pubmed:issnType |
Electronic
|
| pubmed:volume |
16
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
5008-19
|
| pubmed:meshHeading |
pubmed-meshheading:21694667-Catalysis,
pubmed-meshheading:21694667-Ketones,
pubmed-meshheading:21694667-Kinetics,
pubmed-meshheading:21694667-Lithium,
pubmed-meshheading:21694667-Nuclear Magnetic Resonance, Biomolecular,
pubmed-meshheading:21694667-Oxidation-Reduction,
pubmed-meshheading:21694667-Stereoisomerism
|
| pubmed:year |
2011
|
| pubmed:articleTitle |
Enantioselective Evans-Tishchenko reduction of ?-hydroxyketone catalyzed by lithium binaphtholate.
|
| pubmed:affiliation |
Graduate School of Pharmaceutical Sciences, Kumamoto University, 5-1 Oe-honmachi, Kumamoto, Japan.
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| pubmed:publicationType |
Journal Article
|