Catalyst-free cycloaddition of 1,3-diene-1-carbamates with azodicarboxylates: A rapid click reaction.

Affiliation

Institut de Chimie des Substances Naturelles CNRS, Universite Paris-Sud, Universite Paris-Saclay, 1 Avenue de la Terrasse, 91198 Gif-sur-Yvette Cedex, France. Electronic address: [Email]

Abstract

Novel click reactions are of continued interest in many scientific research areas and applications. Herein, we report a novel practical, catalyst-free, azo-Diels-Alder reaction between dienecarbamates and azodicarboxylates exhibiting a remarkable functional group tolerance. The availability of starting materials, mild reaction conditions, chemoselectivity and scalability make this cycloaddition a viable supplement to the other reactions in "click" chemistry.

Keywords

Azodicarboxylate,Click chemistry,Diels-Alder reaction,Heterocycles,Hydropyridazine,

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