Source:http://linkedlifedata.com/resource/pubmed/id/15326529
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
17
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pubmed:dateCreated |
2004-8-24
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pubmed:abstractText |
The first total syntheses of the title fungal metabolites preussomerins F, K and L are described and their structures confirmed thereby. The syntheses were achieved following a versatile, unified, non-biomimetic approach, which is easily extendable to prepare other known and novel members of this family. Key steps include the functionalisation of a 2-arylacetal anion, tandem one-pot Friedel-Crafts cyclisation-deprotection, regioselective substrate-directable hydrogenation and reductive-opening of epoxides.
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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:month |
Sep
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pubmed:issn |
1477-0520
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pubmed:author | |
pubmed:copyrightInfo |
Copyright 2004 The Royal Society of Chemistry
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pubmed:issnType |
Print
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pubmed:day |
7
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pubmed:volume |
2
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2483-95
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pubmed:meshHeading | |
pubmed:year |
2004
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pubmed:articleTitle |
A versatile, non-biomimetic route to the preussomerins: syntheses of (+/-)-preussomerins F, K and L.
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pubmed:affiliation |
Department of Chemistry, University of York, Heslington, York, UKYO10 5DD.
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pubmed:publicationType |
Journal Article
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