Palladium-Catalyzed Amidation of N-Tosylhydrazones with Isocyanides

Aminocarbonylation of N‐tosylhydrazones: The direct formation of ketenimines from carbenes and isocyanides is limited to the reaction of Fischer carbene complexes or some specially stabilized carbenes with isocyanides. A Pd‐catalyzed amidation of N‐tosylhydrazones with isocyanides via a ketenimine i...

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Veröffentlicht in:Chemistry : a European journal 2011-10, Vol.17 (44), p.12268-12271
Hauptverfasser: Zhou, Fengtao, Ding, Ke, Cai, Qian
Format: Artikel
Sprache:eng
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Zusammenfassung:Aminocarbonylation of N‐tosylhydrazones: The direct formation of ketenimines from carbenes and isocyanides is limited to the reaction of Fischer carbene complexes or some specially stabilized carbenes with isocyanides. A Pd‐catalyzed amidation of N‐tosylhydrazones with isocyanides via a ketenimine intermediate in the presence of water is described. The method offers a general way to synthesize amides from carbonyl compounds through one‐carbon extension (see scheme).
ISSN:0947-6539
1521-3765
DOI:10.1002/chem.201102459