Copper-Catalyzed Preparation of γ-Alkylidenebutenolides and Isocoumarins under Mild Palladium-Free Conditions - MédiHAL Accéder directement au contenu
Image (Illustration) Année : 2009

Copper-Catalyzed Preparation of γ-Alkylidenebutenolides and Isocoumarins under Mild Palladium-Free Conditions

Résumé

A general and efficient copper(I)-catalyzed cross-coupling and heterocyclization reaction of terminal alkynes and β-iodo-α,β-unsaturated acid derivatives has been developed under very mild conditions. This method provides easy access from good to excellent yields of a variety of 5-ylidenebutenolides and 3-substituted isocoumarins with excellent regio- and stereoselectivity. This procedure does not require the use of any expensive supplementary additives, and is palladium-free.

Domaines

Chimie organique

Dates et versions

medihal-01727579 , version 1 (09-03-2018)

Licence

Domaine public

Identifiants

  • HAL Id : medihal-01727579 , version 1

Citer

Samuel Inack-Ngi, Raphaël Rahmani, Laurent Commeiras, Gaëlle Chouraqui, Jérôme Thibonnet, et al.. Copper-Catalyzed Preparation of γ-Alkylidenebutenolides and Isocoumarins under Mild Palladium-Free Conditions. Illustration. France. 2009. ⟨medihal-01727579⟩
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