Source:http://linkedlifedata.com/resource/pubmed/id/11463301
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
15
|
| pubmed:dateCreated |
2001-7-20
|
| pubmed:abstractText |
[reaction: see text] In the course of natural product synthetic studies, 5-(4-pentenyl)oxazole and 5-(5-hexenyl)oxazole were N-methylated. The initial N-methylated 5-alkenyloxazolium salt adducts were found to be only intermediates and were ultimately transformed into hydroindole and hydroisoquinoline compounds, respectively.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:month |
Jul
|
| pubmed:issn |
1523-7060
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:day |
26
|
| pubmed:volume |
3
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
2301-3
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| pubmed:dateRevised |
2006-11-15
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| pubmed:meshHeading |
pubmed-meshheading:11463301-Crystallography, X-Ray,
pubmed-meshheading:11463301-Indoles,
pubmed-meshheading:11463301-Isoquinolines,
pubmed-meshheading:11463301-Magnetic Resonance Spectroscopy,
pubmed-meshheading:11463301-Methylation,
pubmed-meshheading:11463301-Molecular Structure,
pubmed-meshheading:11463301-Oxazoles
|
| pubmed:year |
2001
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| pubmed:articleTitle |
N-methylated 5-alkenyloxazolium salt transformations.
|
| pubmed:affiliation |
Department of Chemistry, University of North Texas, Denton, Texas 76203-5068, USA. wenkert@msu.edu
|
| pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|