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 |
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Hauptverfasser: | , , |
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). |
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ISSN: | 0947-6539 1521-3765 |
DOI: | 10.1002/chem.201102459 |