Catalyst-free synthesis of oxazol-2(3H)-ones from sulfilimines and diazo compounds through a tandem rearrangement/aziridination/ring-expansion reaction

Oxazol-2(3H)-ones play a significant role in the fields of organic synthesis and drug development. The classical synthesis of oxazol-2(3H)-one derivatives requires high temperatures, metal catalysts, complex substrates or multi-step reactions. We report a concise synthesis of oxazol-2(3H)-ones from...

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Hauptverfasser: Song, Lina (VerfasserIn) , Tian, Xianhai (VerfasserIn) , Han, Chunyu (VerfasserIn) , Amanpur, Mehran (VerfasserIn) , Rominger, Frank (VerfasserIn) , Hashmi, A. Stephen K. (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 16 Apr 2021
In: Organic chemistry frontiers
Year: 2021, Jahrgang: 8, Heft: 13, Pages: 3314-3319
ISSN:2052-4129
DOI:10.1039/D1QO00473E
Online-Zugang:Resolving-System, lizenzpflichtig, Volltext: https://doi.org/10.1039/D1QO00473E
Verlag, lizenzpflichtig, Volltext: https://pubs.rsc.org/en/content/articlelanding/2021/qo/d1qo00473e
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Verfasserangaben:Lina Song, Xianhai Tian, Chunyu Han, Mehran Amanpur, Frank Rominger and A. Stephen K. Hashmi
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Zusammenfassung:Oxazol-2(3H)-ones play a significant role in the fields of organic synthesis and drug development. The classical synthesis of oxazol-2(3H)-one derivatives requires high temperatures, metal catalysts, complex substrates or multi-step reactions. We report a concise synthesis of oxazol-2(3H)-ones from readily available diazo compounds and sulfilimines through a tandem rearrangement/aziridination/ring-expansion reaction in the absence of any catalyst and additive. This reaction is scalable and the obtained products were readily converted to other valuable aza-heterocyclic frameworks.
Beschreibung:Gesehen am 07.05.2021
Beschreibung:Online Resource
ISSN:2052-4129
DOI:10.1039/D1QO00473E