TfOH catalyzed One-Pot Schmidt–Ritter reaction for the synthesis of amides through N-acylimides

dc.contributor.author Singh, Garima
dc.contributor.author Dada, Ravikrishna
dc.contributor.author Yaragorla, Srinivasarao
dc.date.accessioned 2022-03-27T08:50:00Z
dc.date.available 2022-03-27T08:50:00Z
dc.date.issued 2016-01-01
dc.description.abstract A One-Pot tandem Schmidt–Ritter process for the synthesis of amides has been developed using the super acid as catalyst. The in situ generated aryl/aliphatic nitriles from the reaction of aldehydes and sodium azide in the presence of TfOH and AcOH (Schmidt reaction) react with suitable alcohol (Ritter reaction) to give the amides. For the first time we observed that during the Schmidt process N-acylimides were generated along with nitriles, interestingly these N-acylimides also participated in the Ritter reaction.
dc.identifier.citation Tetrahedron Letters. v.57(39)
dc.identifier.issn 00404039
dc.identifier.uri 10.1016/j.tetlet.2016.08.069
dc.identifier.uri https://www.sciencedirect.com/science/article/abs/pii/S0040403916310966
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/11896
dc.subject Amides
dc.subject Multicomponent reaction
dc.subject N-Acylimides
dc.subject Schmidt–Ritter reaction
dc.subject TfOH
dc.title TfOH catalyzed One-Pot Schmidt–Ritter reaction for the synthesis of amides through N-acylimides
dc.type Journal. Article
dspace.entity.type
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