Source:http://linkedlifedata.com/resource/pubmed/id/17109057
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
45
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pubmed:dateCreated |
2006-11-19
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pubmed:abstractText |
A new organocatalytic system, novel chiral bisformamide and in situ generated L-proline-derived allylsilane reagent , which converts different aldimines to homoallylic amines in good to high yields (up to 95%) and good enantioselectivities (up to 85% ee) has been described.
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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 |
Dec
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pubmed:issn |
1359-7345
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
7
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
4747-9
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pubmed:meshHeading |
pubmed-meshheading:17109057-Alkenes,
pubmed-meshheading:17109057-Aminophenols,
pubmed-meshheading:17109057-Catalysis,
pubmed-meshheading:17109057-Formamides,
pubmed-meshheading:17109057-Magnetic Resonance Spectroscopy,
pubmed-meshheading:17109057-Mass Spectrometry,
pubmed-meshheading:17109057-Molecular Structure,
pubmed-meshheading:17109057-Silanes,
pubmed-meshheading:17109057-Stereoisomerism
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pubmed:year |
2006
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pubmed:articleTitle |
First enantioselective organocatalytic allylation of simple aldimines with allyltrichlorosilane.
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pubmed:affiliation |
Institut für Organische und Biomolekulare Chemie der Georg-August-Universität Göttingen, Tammannstrasse 2, 37077, Göttingen, Germany.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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