Please use this identifier to cite or link to this item: 10.3390/ijms222313145
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dc.contributor.authorStrumfs, Boriss-
dc.contributor.authorHermane, Jekaterina-
dc.contributor.authorBelyakov, Sergey-
dc.contributor.authorSobolevs, Artjoms-
dc.contributor.authorVelikijs, Kirils-
dc.contributor.authorUljanovs, Romans-
dc.contributor.authorTrapencieris, Peteris-
dc.contributor.authorStrumfa, Ilze-
dc.date.accessioned2021-12-30T15:05:02Z-
dc.date.available2021-12-30T15:05:02Z-
dc.date.issued2021-12-05-
dc.identifier.citationStrumfs , B , Hermane , J , Belyakov , S , Sobolevs , A , Velikijs , K , Uljanovs , R , Trapencieris , P & Strumfa , I 2021 , ' An easy route to aziridine ketones and carbinols ' , International Journal of Molecular Sciences , vol. 22 , no. 23 , 13145 . https://doi.org/10.3390/ijms222313145-
dc.identifier.issn1661-6596-
dc.identifier.urihttps://dspace.rsu.lv/jspui/handle/123456789/7147-
dc.descriptionFunding Information: Funding: This research was funded by the European Regional Development Fund, project No. 1.1.1.2/VIAA/1/16/242. The APC was funded by Riga Stradins University, Riga, Latvia. Publisher Copyright: © 2021 by the authors. Licensee MDPI, Basel, Switzerland.-
dc.description.abstractN,N-Dimethylaziridine-2-carboxamides react with organolithium reagents yielding 2-aziridinylketones. The reaction with one equivalent of organolithium compound is selective to amide carbonyl at a low (−78◦C) temperature. These ketones, in reaction with organolithium reagents, give symmetrical and unsymmetrical aziridinyl carbinols. The usage of excess phenyllithium may serve as a special N-Boc-protecting group cleavage method for acid-sensitive substrates.en
dc.format.extent10-
dc.format.extent1730311-
dc.language.isoeng-
dc.relation.ispartofInternational Journal of Molecular Sciences-
dc.rightsinfo:eu-repo/semantics/openAccess-
dc.subjectAziridines-
dc.subjectCarbinols-
dc.subjectKetones-
dc.subjectOrganolithium reagents-
dc.subjectRegioselectivity-
dc.subjectTertiary amides-
dc.subject1.4 Chemical sciences-
dc.subject1.1. Scientific article indexed in Web of Science and/or Scopus database-
dc.subjectCatalysis-
dc.subjectMolecular Biology-
dc.subjectSpectroscopy-
dc.subjectComputer Science Applications-
dc.subjectPhysical and Theoretical Chemistry-
dc.subjectOrganic Chemistry-
dc.subjectInorganic Chemistry-
dc.titleAn easy route to aziridine ketones and carbinolsen
dc.type/dk/atira/pure/researchoutput/researchoutputtypes/contributiontojournal/article-
dc.identifier.doi10.3390/ijms222313145-
dc.contributor.institutionDepartment of Pathology-
dc.contributor.institutionFaculty of Medicine-
dc.identifier.urlhttp://www.scopus.com/inward/record.url?scp=85120580986&partnerID=8YFLogxK-
dc.description.statusPeer reviewed-
Appears in Collections:Research outputs from Pure / Zinātniskās darbības rezultāti no ZDIS Pure

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