Please use this identifier to cite or link to this item:
10.3390/ijms222313145
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DC Field | Value | Language |
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dc.contributor.author | Strumfs, Boriss | - |
dc.contributor.author | Hermane, Jekaterina | - |
dc.contributor.author | Belyakov, Sergey | - |
dc.contributor.author | Sobolevs, Artjoms | - |
dc.contributor.author | Velikijs, Kirils | - |
dc.contributor.author | Uljanovs, Romans | - |
dc.contributor.author | Trapencieris, Peteris | - |
dc.contributor.author | Strumfa, Ilze | - |
dc.date.accessioned | 2021-12-30T15:05:02Z | - |
dc.date.available | 2021-12-30T15:05:02Z | - |
dc.date.issued | 2021-12-05 | - |
dc.identifier.citation | Strumfs , 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.issn | 1661-6596 | - |
dc.identifier.uri | https://dspace.rsu.lv/jspui/handle/123456789/7147 | - |
dc.description | Funding 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.abstract | N,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.extent | 10 | - |
dc.format.extent | 1730311 | - |
dc.language.iso | eng | - |
dc.relation.ispartof | International Journal of Molecular Sciences | - |
dc.rights | info:eu-repo/semantics/openAccess | - |
dc.subject | Aziridines | - |
dc.subject | Carbinols | - |
dc.subject | Ketones | - |
dc.subject | Organolithium reagents | - |
dc.subject | Regioselectivity | - |
dc.subject | Tertiary amides | - |
dc.subject | 1.4 Chemical sciences | - |
dc.subject | 1.1. Scientific article indexed in Web of Science and/or Scopus database | - |
dc.subject | Catalysis | - |
dc.subject | Molecular Biology | - |
dc.subject | Spectroscopy | - |
dc.subject | Computer Science Applications | - |
dc.subject | Physical and Theoretical Chemistry | - |
dc.subject | Organic Chemistry | - |
dc.subject | Inorganic Chemistry | - |
dc.title | An easy route to aziridine ketones and carbinols | en |
dc.type | /dk/atira/pure/researchoutput/researchoutputtypes/contributiontojournal/article | - |
dc.identifier.doi | 10.3390/ijms222313145 | - |
dc.contributor.institution | Department of Pathology | - |
dc.contributor.institution | Faculty of Medicine | - |
dc.identifier.url | http://www.scopus.com/inward/record.url?scp=85120580986&partnerID=8YFLogxK | - |
dc.description.status | Peer reviewed | - |
Appears in Collections: | Research outputs from Pure / Zinātniskās darbības rezultāti no ZDIS Pure |
Files in This Item:
File | Size | Format | |
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An_Easy_Route_to_Aziridine_Ketones_and_Carbinols.pdf | 1.69 MB | Adobe PDF | View/Open |
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