Asymmetric iodocyclization of gamma-hydroxyalkenes

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dc.contributor.authorKang, SungHoko
dc.contributor.authorPark, CMko
dc.contributor.authorLee, SBko
dc.contributor.authorKim, Mko
dc.date.accessioned2013-03-04T13:43:17Z-
dc.date.available2013-03-04T13:43:17Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2004-06-
dc.identifier.citationSYNLETT, v.126, pp.1279 - 1281-
dc.identifier.issn0936-5214-
dc.identifier.urihttp://hdl.handle.net/10203/82821-
dc.description.abstractEnantioselective intramolecular iodoetherification of disubstituted gamma-hydroxyalkenes has been intended using NIS in the presence of 0.2 equivalents of (R)-Binol-Ti(IV) complex to procure the corresponding tetrahydrofurans in up to 65% ee.-
dc.languageEnglish-
dc.publisherGEORG THIEME VERLAG KG-
dc.subjectHOST-GUEST COMPLEXATION-
dc.subjectEFFICIENT PREPARATION-
dc.subjectCYCLIZATION-
dc.subjectALDEHYDES-
dc.subjectZEOLITES-
dc.titleAsymmetric iodocyclization of gamma-hydroxyalkenes-
dc.typeArticle-
dc.identifier.wosid000222705200034-
dc.identifier.scopusid2-s2.0-2942724617-
dc.type.rimsART-
dc.citation.volume126-
dc.citation.beginningpage1279-
dc.citation.endingpage1281-
dc.citation.publicationnameSYNLETT-
dc.identifier.doi10.1055/s-2004-825593-
dc.contributor.localauthorKang, SungHo-
dc.contributor.nonIdAuthorPark, CM-
dc.contributor.nonIdAuthorLee, SB-
dc.contributor.nonIdAuthorKim, M-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorreagent-controlled-
dc.subject.keywordAuthoriodocyclization-
dc.subject.keywordAuthorgamma-hydroxyalkenes-
dc.subject.keywordAuthor(R)-Binol-Ti(IV) complex-
dc.subject.keywordAuthorN-iodosuccinimide-
dc.subject.keywordPlusHOST-GUEST COMPLEXATION-
dc.subject.keywordPlusEFFICIENT PREPARATION-
dc.subject.keywordPlusCYCLIZATION-
dc.subject.keywordPlusALDEHYDES-
dc.subject.keywordPlusZEOLITES-
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