Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
17
pubmed:dateCreated
2004-8-24
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.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
1477-0520
pubmed:author
pubmed:copyrightInfo
Copyright 2004 The Royal Society of Chemistry
pubmed:issnType
Print
pubmed:day
7
pubmed:volume
2
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2483-95
pubmed:meshHeading
pubmed:year
2004
pubmed:articleTitle
A versatile, non-biomimetic route to the preussomerins: syntheses of (+/-)-preussomerins F, K and L.
pubmed:affiliation
Department of Chemistry, University of York, Heslington, York, UKYO10 5DD.
pubmed:publicationType
Journal Article