Source:http://linkedlifedata.com/resource/pubmed/id/21581973
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Predicate | Object |
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rdf:type | |
pubmed:issue |
Pt 2
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pubmed:dateCreated |
2011-5-17
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pubmed:abstractText |
The title compound, C(19)H(17)ClN(2)O(5)S, was synthesized by the reaction of ethyl 6-(4-chloro-phen-yl)-2-mercapto-4-methyl-1,6-dihydro-pyrimidine-5-carboxyl-ate and dimethyl acetyl-ene-dicarboxyl-ate in methanol. In the mol-ecule, the nearly planar thia-zole ring, with a mean deviation from the plane of 0.0108?(3)?Å, is fused with a dihydro-pyrimidine ring in a flattened half-chair conformation.
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/21581973-17070617,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21581973-17148913,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21581973-18156677,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21581973-2041050
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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 |
65
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
o375
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pubmed:dateRevised |
2011-11-11
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pubmed:year |
2009
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pubmed:articleTitle |
Ethyl 5-(4-chloro-phen-yl)-2-[(Z)-(methoxy-carbon-yl)methyl-ene]-7-methyl-3-oxo-3,5-dihydro-2H-thia-zolo[3,2-a]pyrimi-dine-6-carboxyl-ate.
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pubmed:publicationType |
Journal Article
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