Issue 60, 2021

Iridium-catalysed branched-selective hydroacylation of 1,3-dienes with salicylaldehydes

Abstract

Herein, we report an iridium-catalyzed branched-selective hydroacylation of 1-aryl 1,3-dienes with salicylaldehydes under mild conditions with no need of phosphine ligands. With this protocol, a series of α-branched β,γ-unsaturated o-hydroxyacetophenones with biological potentials were synthesized in high efficiency with excellent regioselectivities. When simple 1,3-butadiene or isoprene instead of 1-aryl 1,3-dienes were used, exclusive linear-selective hydroacylation products were obtained.

Graphical abstract: Iridium-catalysed branched-selective hydroacylation of 1,3-dienes with salicylaldehydes

Supplementary files

Article information

Article type
Communication
Submitted
08 Apr 2021
Accepted
29 Jun 2021
First published
30 Jun 2021

Chem. Commun., 2021,57, 7378-7381

Iridium-catalysed branched-selective hydroacylation of 1,3-dienes with salicylaldehydes

Y. Yang and D. Xing, Chem. Commun., 2021, 57, 7378 DOI: 10.1039/D1CC01872H

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