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A useful synthetic equivalent of an acetone enolate

dc.creatorMaslak, Veselin
dc.creatorTokić-Vujošević, Zorana
dc.creatorFerjancić, Zorana
dc.creatorSaičić, Radomir N.
dc.date.accessioned2019-09-02T11:16:58Z
dc.date.available2019-09-02T11:16:58Z
dc.date.issued2009
dc.identifier.issn0040-4039
dc.identifier.urihttps://farfar.pharmacy.bg.ac.rs/handle/123456789/1204
dc.description.abstract2-Methoxymethoxy-3-chloropropene derived organometallics act as synthetic equivalents of an acetone enolate. Indium-promoted reaction of this reagent with aldehydes affords aldol adducts in moderate to excellent yields. When the reaction was performed with zinc, aldol products were isolated in protected form as the corresponding MOM-enol ethers.en
dc.publisherPergamon-Elsevier Science Ltd, Oxford
dc.relationinfo:eu-repo/grantAgreement/MESTD/MPN2006-2010/142021/RS//
dc.rightsrestrictedAccess
dc.sourceTetrahedron-Asymmetry
dc.subjectAllylationen
dc.subjectAldehydesen
dc.subjectIndiumen
dc.subjectZincen
dc.subjectAldol reactionen
dc.subjectWateren
dc.titleA useful synthetic equivalent of an acetone enolateen
dc.typearticle
dc.rights.licenseARR
dcterms.abstractМаслак, Веселин; Ферјанцић, Зорана; Саичић, Радомир Н.; Токић-Вујошевић, Зорана;
dc.citation.volume50
dc.citation.issue48
dc.citation.spage6709
dc.citation.epage6711
dc.citation.other50(48): 6709-6711
dc.citation.rankM22
dc.identifier.wos000271410800025
dc.identifier.doi10.1016/j.tetlet.2009.09.113
dc.identifier.scopus2-s2.0-70349992636
dc.type.versionpublishedVersion


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