Source:http://linkedlifedata.com/resource/pubmed/id/18159933
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2008-1-14
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pubmed:abstractText |
A microwave-assisted protocol was developed for the construction of di- and monosubstituted 2-aminoimidazoles. The two-step reaction involves the synthesis of N-(1H-imidazol-2-yl)acetamides from readily available alpha-haloketones and N-acetylguanidine, followed by deacetylation. Significant rate enhancement was observed for both steps of the protocol, and the overall reaction time was shortened to 20 min compared to 48 h of the conventional procedures. A representative set of di- and monosubstituted 2-aminoimidazoles was prepared using commercially available parallel reactors.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:issn |
1520-4774
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
10
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
118-22
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pubmed:meshHeading | |
pubmed:articleTitle |
An efficient and expeditious synthesis of di- and monosubstituted 2-aminoimidazoles.
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pubmed:affiliation |
Department of Chemistry, National University of Singapore, 3 Science Drive 3, Singapore.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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