New versatile approach to alpha-hydrazonoesters and amino acid derivatives through a modified Japp-Klingemann reaction

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.

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Bibliographic Details
Published inChemical communications (Cambridge, England) no. 15; pp. 1385 - 1386
Main Authors Atlan, El Kaim, L, Supiot, C
Format Journal Article
LanguageEnglish
Published CAMBRIDGE Royal Soc Chemistry 01.01.2000
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