Issue 6, 2020

Facile access to versatile aza-macrolides through iridium-catalysed cascade allyl-amination/macrolactonization

Abstract

Direct access to benzo-fused aza-macrolides was successfully achieved through iridium-catalysed intermolecular decarboxylative coupling of vinylethylene carbonates with isatoic anhydrides under relatively mild reaction conditions. Notably, this reaction proceeded through sequential allyl-amination/macrolactonization upon extrusion of CO2. Moreover, favourable fluorescence properties could be observed in the title macrocyclic products.

Graphical abstract: Facile access to versatile aza-macrolides through iridium-catalysed cascade allyl-amination/macrolactonization

Supplementary files

Article information

Article type
Communication
Submitted
19 Sep 2019
Accepted
06 Dec 2019
First published
06 Dec 2019

Chem. Commun., 2020,56, 960-963

Facile access to versatile aza-macrolides through iridium-catalysed cascade allyl-amination/macrolactonization

W. Fu, L. Wang, Z. Yang, J. Shen, F. Tang, J. Zhang and X. Cui, Chem. Commun., 2020, 56, 960 DOI: 10.1039/C9CC07372H

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