Source:http://linkedlifedata.com/resource/pubmed/id/14535721
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
21
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pubmed:dateCreated |
2003-10-10
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pubmed:abstractText |
[reaction: see text] New monodentate phosphite ligands have been developed from axially chiral biphenols, which show excellent enantioselectivity in the Rh(I)-catalyzed hydrogenation of dimethyl itaconate. The new chiral ligand system is suitable to create libraries and possesses fine-tuning capability.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1523-7060
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
16
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pubmed:volume |
5
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
3831-4
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:14535721-Catalysis,
pubmed-meshheading:14535721-Hydrogenation,
pubmed-meshheading:14535721-Ligands,
pubmed-meshheading:14535721-Models, Chemical,
pubmed-meshheading:14535721-Molecular Structure,
pubmed-meshheading:14535721-Phosphites,
pubmed-meshheading:14535721-Rhodium,
pubmed-meshheading:14535721-Stereoisomerism
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pubmed:year |
2003
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pubmed:articleTitle |
Synthesis of new chiral monodentate phosphite ligands and their use in catalytic asymmetric hydrogenation.
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pubmed:affiliation |
Department of Chemistry, State University of New York at Stony Brook, Stony Brook, New York 11794-3400, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, Non-U.S. Gov't
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