Journal
ORGANIC LETTERS
Volume 16, Issue 20, Pages 5332-5335Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol502515b
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Funding
- Universita del Piemonte Orientale
- Progetto Strain-Regione Campania
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A novel one-pot multicomponent synthesis of alpha-ammo carbonyl N-acylhydrazones starting from readily available hydrazonoyl chlorides, isocyanides, and carboxylic acids is reported. The strategy exploits the ability of the carboxylic acid as third component to suppress all competing reactions between nitrile imines and isocyanides, channeling the course of the reaction toward the formation of this novel class of compounds.
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