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A useful synthetic equivalent of an acetone enolate

dc.creatorMaslak, Veselin
dc.creatorTokić-Vujošević, Zorana
dc.creatorFerjančić, Zorana
dc.creatorSaičić, Radomir
dc.date.accessioned2018-11-22T00:15:21Z
dc.date.available2018-11-22T00:15:21Z
dc.date.issued2009
dc.identifier.issn0040-4039
dc.identifier.urihttps://cherry.chem.bg.ac.rs/handle/123456789/1026
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. (C) 2009 Elsevier Ltd. All rights reserved.en
dc.publisherPergamon-Elsevier Science Ltd, Oxford
dc.relationinfo:eu-repo/grantAgreement/MESTD/MPN2006-2010/142021/RS//
dc.rightsrestrictedAccess
dc.sourceTetrahedron Letters
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.abstractСаичић, Радомир; Ферјанчић, Зорана; Маслак, Веселин; Токиц-Вујосевиц, Зорана;
dc.citation.volume50
dc.citation.issue48
dc.citation.spage6709
dc.citation.epage6711
dc.identifier.wos000271410800025
dc.identifier.doi10.1016/j.tetlet.2009.09.113
dc.citation.other50(48): 6709-6711
dc.citation.rankM22
dc.type.versionpublishedVersionen
dc.identifier.scopus2-s2.0-70349992636


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