Issue 17, 2021

Gold(iii)-catalyzed bicyclizations of alkylidenecyclopropane-tethered ynones for divergent synthesis of indene and naphthalenone-based polycycles

Abstract

A gold(III)-catalyzed cascade oxidation/cyclization of alkylidenecyclopropane-tethered ynones for the assembly of diverse polycycles by employing different N-oxides with distinct nucleophilic properties is reported. This protocol enables the synthesis of cyclopentene-fused indenes and cyclobutane-fused naphthalenones in moderate to excellent yields using common starting materials in the presence of 2,6-Cl2-pyridine N-oxide as an indispensable co-ligand of the gold(III) catalyst and 8-Me-quinoline N-oxide as an oxidant, respectively. Notably, compound 3h showed promising antibacterial activity against R. solanacearum (MIC = 2 μg mL−1), and its preliminary antibacterial mechanism was also explored.

Graphical abstract: Gold(iii)-catalyzed bicyclizations of alkylidenecyclopropane-tethered ynones for divergent synthesis of indene and naphthalenone-based polycycles

Supplementary files

Article information

Article type
Research Article
Submitted
29 May 2021
Accepted
24 Jun 2021
First published
25 Jun 2021

Org. Chem. Front., 2021,8, 4853-4859

Gold(III)-catalyzed bicyclizations of alkylidenecyclopropane-tethered ynones for divergent synthesis of indene and naphthalenone-based polycycles

J. Li, H. Huo, F. Yang, Q. Zhou, M. Li, Z. Chen and K. Ji, Org. Chem. Front., 2021, 8, 4853 DOI: 10.1039/D1QO00821H

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