DIRECT FACILE TETRAHYDROFURANYLATION OF ALCOHOLS THROUGH RADICAL COUPLING WITH (BU4N)2S2O8

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dc.contributor.authorJ. C. Jungko
dc.contributor.authorKim, Yong Haeko
dc.date.accessioned2013-02-25T15:45:32Z-
dc.date.available2013-02-25T15:45:32Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued1993-
dc.identifier.citationTETRAHEDRON LETTERS, v.34, no.22, pp.3581 - 3584-
dc.identifier.issn0040-4039-
dc.identifier.urihttp://hdl.handle.net/10203/63304-
dc.description.abstractPrimary, secondary and tertiary alcohols can be converted in excellent yields into their 2-tetrahydrofuranyl-ethers in the presence of n-tetrabutylammonium peroxydisulfate1 under nearly neutral condition in tetrahydrofuran.-
dc.languageEnglish-
dc.publisherPergamon-Elsevier Science Ltd-
dc.subjectPEROXYDISULFATE-
dc.subjectOXIDATION-
dc.titleDIRECT FACILE TETRAHYDROFURANYLATION OF ALCOHOLS THROUGH RADICAL COUPLING WITH (BU4N)2S2O8-
dc.typeArticle-
dc.identifier.wosidA1993LE30100022-
dc.identifier.scopusid2-s2.0-0027300442-
dc.type.rimsART-
dc.citation.volume34-
dc.citation.issue22-
dc.citation.beginningpage3581-
dc.citation.endingpage3584-
dc.citation.publicationnameTETRAHEDRON LETTERS-
dc.contributor.nonIdAuthorJ. C. Jung-
dc.type.journalArticleArticle-
dc.subject.keywordPlusPEROXYDISULFATE-
dc.subject.keywordPlusOXIDATION-
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