Issue 15, 2000

New versatile approach to α-hydrazonoesters and amino acid derivatives trough a modified Japp–Klingemann reaction

Abstract

Addition of diazonium tetrafluoroborates to an acyl chloride pyridine mixture affords hydrazonoacid derivatives in smooth conditions; this new Japp–Klingemann reaction emphasizes the synthetic potential of electrophilic addition to ketenes.

Article information

Article type
Communication
Submitted
25 Apr 2000
Accepted
22 May 2000
First published
05 Jul 2000

Chem. Commun., 2000, 1385-1386

New versatile approach to α-hydrazonoesters and amino acid derivatives trough a modified Japp–Klingemann reaction

V. Atlan, L. E. Kaim and C. Supiot, Chem. Commun., 2000, 1385 DOI: 10.1039/B003361H

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