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dc.contributor.authorAmonkar, C.P.
dc.contributor.authorTilve, S.G.
dc.contributor.authorParameswaran, P.S.
dc.date.accessioned2008-02-22T04:45:43Z
dc.date.available2008-02-22T04:45:43Z
dc.date.issued2005
dc.identifier.citationSynthesis - Stuttgart, Vol.14; 2341-2344p.
dc.identifier.urihttp://drs.nio.org/drs/handle/2264/887
dc.description.abstractA convenient three-step synthetic approach towards 3-alkyl-5-methyl-2[5H]furanones is described. The steps involved in the synthesis are domino primary alcohol oxidation-Wittig reaction, acid-catalysed lactonisation and isomerisation. This synthetic approach has been exploited to synthesise four Streptomyces lac-tones.
dc.language.isoen
dc.publisherThieme
dc.rightsCopyright [2005]. It is tried to respect the rights of the copyright holders to the best of the knowledge. If it is brought to our notice by copyright holder that the rights are voilated then the item would be withdrawn.
dc.subjectnatural products
dc.subjectchemical analysis
dc.subjectmetabolites
dc.subjectbioactive compounds
dc.subjectmolecular structure
dc.subjectisomerization
dc.subjectoxidation
dc.subjectalcohol
dc.subjectStreptomyces
dc.titleConvenient synthesis of volatile streptomyces lactones
dc.typeJournal Article


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