A STEREOSELECTIVE SYNTHETIC ROUTE TO CIS-2,5-DISUBSTITUTED TETRAHYDROFURANS

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dc.contributor.authorKang, SungHoko
dc.contributor.authorHWANG, TSko
dc.contributor.authorKIM, WJko
dc.contributor.authorLIM, JKko
dc.date.accessioned2013-02-25T23:00:25Z-
dc.date.available2013-02-25T23:00:25Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued1991-08-
dc.identifier.citationTETRAHEDRON LETTERS, v.32, no.32, pp.4015 - 4018-
dc.identifier.issn0040-4039-
dc.identifier.urihttp://hdl.handle.net/10203/65888-
dc.description.abstractAn efficient stereocontrolled synthesis of cis-2,5-disubstituted tetrahydrofurans from triethylsilyl ethers of trans-4-phenyl-3-buten-1-ol derivatives 19-24 was developed by using phenylselenyl chloride in the presence of potassium carbonate in acetonitrile.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectTRANS-2,5-DISUBSTITUTED TETRAHYDROFURANS-
dc.subjectSUBSTITUTED TETRAHYDROFURANS-
dc.subjectPHENYLSELENOETHERIFICATION-
dc.subjectCYCLIZATIONS-
dc.titleA STEREOSELECTIVE SYNTHETIC ROUTE TO CIS-2,5-DISUBSTITUTED TETRAHYDROFURANS-
dc.typeArticle-
dc.identifier.wosidA1991FY85500030-
dc.identifier.scopusid2-s2.0-0025744993-
dc.type.rimsART-
dc.citation.volume32-
dc.citation.issue32-
dc.citation.beginningpage4015-
dc.citation.endingpage4018-
dc.citation.publicationnameTETRAHEDRON LETTERS-
dc.contributor.localauthorKang, SungHo-
dc.contributor.nonIdAuthorHWANG, TS-
dc.contributor.nonIdAuthorKIM, WJ-
dc.contributor.nonIdAuthorLIM, JK-
dc.type.journalArticleArticle-
dc.subject.keywordPlusTRANS-2,5-DISUBSTITUTED TETRAHYDROFURANS-
dc.subject.keywordPlusSUBSTITUTED TETRAHYDROFURANS-
dc.subject.keywordPlusPHENYLSELENOETHERIFICATION-
dc.subject.keywordPlusCYCLIZATIONS-
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