Source:http://linkedlifedata.com/resource/pubmed/id/19137523
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
7
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pubmed:dateCreated |
2009-2-2
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pubmed:abstractText |
Let it flow, let it flow: A procedure to generate the first solid-supported mercuric salt, silaphenylmercuric triflate, is described. Silaphenylmercuric triflate showed remarkable catalytic activity for an indole synthesis, furanoyne cyclization, arylyne cyclization, and tandem carbocyclizations. An efficient flow reaction system for indole synthesis and arylyne cyclization is also described (see figure).
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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/Alkynes,
http://linkedlifedata.com/resource/pubmed/chemical/Heterocyclic Compounds,
http://linkedlifedata.com/resource/pubmed/chemical/Indoles,
http://linkedlifedata.com/resource/pubmed/chemical/Mesylates,
http://linkedlifedata.com/resource/pubmed/chemical/Organomercury Compounds,
http://linkedlifedata.com/resource/pubmed/chemical/indole
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pubmed:status |
MEDLINE
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pubmed:issn |
1521-3773
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
48
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1244-7
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pubmed:meshHeading | |
pubmed:year |
2009
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pubmed:articleTitle |
Silaphenylmercuric triflate catalyzed reactions: synthesis of a solid-supported mercuric salt catalyst.
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pubmed:affiliation |
Faculty of Pharmaceutical Sciences, Tokushima Bunri University, Yamashiro-cho, Tokushima 770-8514, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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