Source:http://linkedlifedata.com/resource/pubmed/id/11348224
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
9
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pubmed:dateCreated |
2001-5-11
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pubmed:abstractText |
[structure in text] The synthesis of several 4-vinylimidazoles via Stille cross-coupling reactions of the corresponding protected 4-iodoimidazoles with tributylvinylstannane is described. These heterocyclic dienes are shown to be effective partners in the Diels-Alder reaction, providing adducts in good yield and exhibiting useful levels of isomer selectivity and stereoselectivity (endo/exo).
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pubmed:language |
eng
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pubmed:journal | |
pubmed:status |
PubMed-not-MEDLINE
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pubmed:month |
May
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pubmed:issn |
1523-7060
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
3
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pubmed:volume |
3
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1319-22
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pubmed:dateRevised |
2003-10-31
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pubmed:year |
2001
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pubmed:articleTitle |
Synthesis and Diels-Alder reactions of 4-vinylimidazoles.
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pubmed:affiliation |
Department of Chemistry and Biochemistry, The University of Texas at Arlington, Arlington, Texas 76019, USA. lovely@uta.edu
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pubmed:publicationType |
Journal Article
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