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dc.creatorBigović, Miljan
dc.creatorMaslak, Veselin
dc.creatorTokić-Vujošević, Zorana
dc.creatorDivjaković, Vladimir
dc.creatorSaičić, Radomir
dc.date.accessioned2018-11-22T00:18:43Z
dc.date.available2018-11-22T00:18:43Z
dc.date.issued2011
dc.identifier.issn1523-7060
dc.identifier.urihttp://cherry.chem.bg.ac.rs/handle/123456789/1194
dc.description.abstractIndium promoted allyiation of carbonyl compounds with 4-(bromomethyl)-1,3-dioxol-2-one diastereoselectively affords and-alpha,beta-dihydroxyketones, protected as enol carbonates. These initial products can be deprotected to free dihydroxyketones or transformed under mild conditions Into the corresponding cyclic carbonates, which constitutes a useful approach to hydroxyacetone aldois.en
dc.publisherAmer Chemical Soc, Washington
dc.relationinfo:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/172027/RS//
dc.rightsrestrictedAccess
dc.sourceOrganic Letters
dc.titleA Useful Synthetic Equivalent of a Hydroxyacetone Enolateen
dc.typearticle
dc.rights.licenseARR
dcterms.abstractБиговиц, Миљан; Дивјаковиц, Владимир; Токиц-Вујосевиц, Зорана; Саичић, Радомир; Маслак, Веселин;
dc.citation.volume13
dc.citation.issue17
dc.citation.spage4720
dc.citation.epage4723
dc.identifier.wos000294242600062
dc.identifier.doi10.1021/ol2019357
dc.citation.other13(17): 4720-4723
dc.citation.rankM21
dc.identifier.pmid21815664
dc.description.otherSupplementary material: [http://cherry.chem.bg.ac.rs/handle/123456789/3570]
dc.type.versionpublishedVersionen
dc.identifier.scopus2-s2.0-80052215702
dc.identifier.rcubKon_2216


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