Issue 17, 2023

Chelation-assisted iridium-catalyzed hydroalkenylation and hydroarylation/cyclization with conjugated trienes

Abstract

Iridium-catalyzed hydroalkenylation of conjugated trienes by chelation-assisted alkenyl C–H activation of acrylamides has been demonstrated to produce 1,4,6-trienes atom efficiently with excellent regio- and E/Z selectivities. In contrast, the reaction of benzamides and 1,3,5-trienes proceeds by a tandem hydroarylation of the trienes and cyclization via intramolecular 1,2-addition, providing valuable trans-tetrahydroisoquinolinone derivatives. A broad range of aromatic and aliphatic 1,3,5-trienes bearing various functionalities were compatible to deliver target products with high yields and E/Z selectivity. The successful gram-scale preparation and selective hydrogenation to give the alkylation product further demonstrates the practicability of this protocol to potential applications.

Graphical abstract: Chelation-assisted iridium-catalyzed hydroalkenylation and hydroarylation/cyclization with conjugated trienes

Supplementary files

Article information

Article type
Communication
Submitted
03 Feb 2023
Accepted
30 Mar 2023
First published
12 Apr 2023

Org. Biomol. Chem., 2023,21, 3537-3541

Chelation-assisted iridium-catalyzed hydroalkenylation and hydroarylation/cyclization with conjugated trienes

Y. Liao, C. Zhang, Y. Wang, Y. Hu, L. Ding, L. Zhong, G. Zhong and J. Zhang, Org. Biomol. Chem., 2023, 21, 3537 DOI: 10.1039/D3OB00166K

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