Source:http://linkedlifedata.com/resource/pubmed/id/21202555
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| Predicate | Object |
|---|---|
| rdf:type | |
| pubmed:issue |
Pt 6
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| pubmed:dateCreated |
2011-1-4
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| pubmed:abstractText |
In the title compound, C(18)H(21)BrN(2)O(5), conjugation between the ?-donating N-C-O fragment and the ?-withdrawing carbonyl group results in considerable redistribution of the electron density within the dihydropyridinol ring. This effect is also promoted by the formation of an intra-molecular N-H?O hydrogen bond. The five-membered heterocycle is disordered over two envelope conformations in a 0.35:0.65 ratio.
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| pubmed:commentsCorrections | |
| pubmed:language |
eng
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| pubmed:journal | |
| pubmed:status |
PubMed-not-MEDLINE
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| pubmed:issn |
1600-5368
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| pubmed:author | |
| pubmed:issnType |
Electronic
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| pubmed:volume |
64
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| pubmed:owner |
NLM
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| pubmed:authorsComplete |
Y
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| pubmed:pagination |
o1031
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| pubmed:dateRevised |
2011-11-11
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| pubmed:year |
2008
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| pubmed:articleTitle |
2-Bromo-methyl-N-isopropyl-7,8-dimeth-oxy-1,2-dihydro-1,3-oxazolo[3,2-a]quinoline-4-carboxamide.
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| pubmed:publicationType |
Journal Article
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