Dephosphonylation of alpha-fully substituted beta-keto phosphonates with LiAlH4; Regioselective alkylation of ketones employing phosphonate as a temporary activating group

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dc.contributor.authorS. Y. Leeko
dc.contributor.authorJ. E. Hongko
dc.contributor.authorW. B. Jangko
dc.contributor.authorOh, Dong Youngko
dc.date.accessioned2013-02-27T23:05:55Z-
dc.date.available2013-02-27T23:05:55Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued1997-
dc.identifier.citationTETRAHEDRON LETTERS, v.38, no.26, pp.4567 - 4570-
dc.identifier.issn0040-4039-
dc.identifier.urihttp://hdl.handle.net/10203/71368-
dc.description.abstractAlkylation of beta-keto phosphonates is performed by treatment of beta-keto phosphonates with n-BuLi, followed by addition of alkyl halides. The acquired a fully substituted beta-keto phosphonates are dephosphonylated by treatment of the lithium enolates with LiAlH4, followed by quenching with aqueous H2SO4 solution. This whole procedure represents a new route to regioselective alkylation of ketones. (C) 1997 Elsevier Science Ltd.-
dc.languageEnglish-
dc.publisherPergamon-Elsevier Science Ltd-
dc.subjectSULFONES-
dc.titleDephosphonylation of alpha-fully substituted beta-keto phosphonates with LiAlH4; Regioselective alkylation of ketones employing phosphonate as a temporary activating group-
dc.typeArticle-
dc.identifier.wosidA1997XG71300013-
dc.identifier.scopusid2-s2.0-0030912336-
dc.type.rimsART-
dc.citation.volume38-
dc.citation.issue26-
dc.citation.beginningpage4567-
dc.citation.endingpage4570-
dc.citation.publicationnameTETRAHEDRON LETTERS-
dc.contributor.nonIdAuthorS. Y. Lee-
dc.contributor.nonIdAuthorJ. E. Hong-
dc.contributor.nonIdAuthorW. B. Jang-
dc.type.journalArticleArticle-
dc.subject.keywordPlusSULFONES-
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