Source:http://linkedlifedata.com/resource/pubmed/id/20953491
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2010-12-24
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pubmed:abstractText |
The synthesis of 8-aminoquinolines and 1,10-phenanthrolines with substituents in ? of the nitrogen has been performed through an inverse-demanding aza-Diels-Alder (Povarov reaction) in the fluoroalcohols TFE or HFIP. This path involves simple starting materials: 1,2-phenylenediamines, enol ethers and aldehydes.
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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 |
Jan
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pubmed:issn |
1477-0539
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:day |
21
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pubmed:volume |
9
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
347-50
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pubmed:meshHeading | |
pubmed:year |
2011
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pubmed:articleTitle |
Synthesis of substituted 8-aminoquinolines and phenanthrolines through a Povarov approach.
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pubmed:affiliation |
Laboratoire BioCIS-CNRS, Faculté de Pharmacie, Univ Paris Sud, 5 rue J.B. Clément, F-92296 Châtenay-Malabry, France.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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