A convenient approach to the synthesis of fused acetal derivatives by tetrabutylammonium peroxydisulfate-mediated oxidative cycloaddition of 1,3-dicarbonyl compounds to cyclic enol ethers: A rebuttal

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dc.contributor.authorJadhav, Vko
dc.contributor.authorPark, MYko
dc.contributor.authorKim, Yong Haeko
dc.date.accessioned2013-03-03T15:42:41Z-
dc.date.available2013-03-03T15:42:41Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2004-02-
dc.identifier.citationSYNTHESIS-STUTTGART, no.3, pp.329 - 330-
dc.identifier.issn0039-7881-
dc.identifier.urihttp://hdl.handle.net/10203/79284-
dc.description.abstractThe report that fused acetal derivatives can be obtained from oxidative cycloaddition of 1,3-diketones or 1,3-diketo esters to cyclic enol ethers using tetrabutyl ammonium peroxydisulfate was proved to be erroneous. Under these reaction conditions fused acetals were neither isolated nor confirmed.-
dc.languageEnglish-
dc.publisherGeorg Thieme Verlag Kg-
dc.subjectN-BUTYLAMMONIUM PEROXYDISULFATE-
dc.subjectORGANIC-SYNTHESIS-
dc.subjectFACILE-
dc.subjectALCOHOLS-
dc.titleA convenient approach to the synthesis of fused acetal derivatives by tetrabutylammonium peroxydisulfate-mediated oxidative cycloaddition of 1,3-dicarbonyl compounds to cyclic enol ethers: A rebuttal-
dc.typeArticle-
dc.identifier.wosid000189230800003-
dc.type.rimsART-
dc.citation.issue3-
dc.citation.beginningpage329-
dc.citation.endingpage330-
dc.citation.publicationnameSYNTHESIS-STUTTGART-
dc.identifier.doi10.1055/s-2004-815930-
dc.contributor.nonIdAuthorJadhav, V-
dc.contributor.nonIdAuthorPark, MY-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorenols-
dc.subject.keywordAuthorethers-
dc.subject.keywordAuthorcycloadditions-
dc.subject.keywordAuthoracetals-
dc.subject.keywordAuthorsulfates-
dc.subject.keywordPlusN-BUTYLAMMONIUM PEROXYDISULFATE-
dc.subject.keywordPlusORGANIC-SYNTHESIS-
dc.subject.keywordPlusFACILE-
dc.subject.keywordPlusALCOHOLS-
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