Synlett 2020; 31(12): 1211-1215
DOI: 10.1055/s-0040-1708015
letter
© Georg Thieme Verlag Stuttgart · New York

Formation of Imidazolones by Ring Closure of α-Isocyanoamides: Exploring New Reactivities

Steven Frippiat
,
Claire Leterrier
,
Christine Baudequin
,
Christophe Hoarau
,
Laurent Bischoff
Normandie University, COBRA, UMR 6014 et FR 3038, University of Rouen; INSA Rouen; CNRS, IRCOF, 1 rue Tesnière, 76821 Mont-Saint-Aignan Cedex, France   eMail: Laurent.bischoff@univ-rouen.fr
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This work has been partially supported by INSA Rouen, Rouen University, CNRS, EFRD, European INTERREG IV A France (Channel) and Labex SynOrg (ANR-11-LABX-0029). S.F. is grateful to the Region Normandie for a grant.
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Publikationsverlauf

Received: 10. März 2020

Accepted after revision: 27. März 2020

Publikationsdatum:
16. April 2020 (online)


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Abstract

Base-mediated ring closure of α,α-disubstituted α-isocyanoamides with further electrophilic trapping has previously been explored, but with limited applications. In this work, we wished to unravel the reactivities of these compounds and, in particular, to allow palladium-catalyzed coupling at the C2 position.

Supporting Information