Source:http://linkedlifedata.com/resource/pubmed/id/20213288
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2010-11-18
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pubmed:abstractText |
A novel multicomponent reaction of isocyanides with thiophenols and gem-diactivated olefins has been discovered. Depending on the choice of isocyanides, substituted 2-aminopyrroles or thioimidates have been prepared. The obtained scaffolds bearing four points of diversity can directly be used in combinatorial syntheses.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Alkenes,
http://linkedlifedata.com/resource/pubmed/chemical/Cyanides,
http://linkedlifedata.com/resource/pubmed/chemical/Phenols,
http://linkedlifedata.com/resource/pubmed/chemical/Pyrroles,
http://linkedlifedata.com/resource/pubmed/chemical/Sulfhydryl Compounds,
http://linkedlifedata.com/resource/pubmed/chemical/thiophenol
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
1573-501X
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
14
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
543-50
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pubmed:meshHeading | |
pubmed:year |
2010
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pubmed:articleTitle |
Reaction of isocyanides with thiophenols and gem-diactivated olefins: a one-pot synthesis of substituted 2-aminopyrroles.
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pubmed:affiliation |
Department of Technology for Organic Synthesis, TOSLab, Ural State Technical University, 620002 Ekaterinburg, Russian Federation.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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