Issue 3, 2024

Synthesis of silyl indenes by ruthenium-catalyzed aldehyde- and acylsilane-enabled C–H alkylation/cyclization

Abstract

A ruthenium-catalyzed C–H alkylation/cyclization sequence is presented to prepare silyl indenes with atom and step-economy. This domino reaction is triggered by acyl silane-directed C–H activation, and an aldehyde controlled the following enol cyclization/condensation other than β-H elimination. The protocol tolerates a broad substitution pattern, and the further synthetic elaboration of silyl indenes allows access to a diverse range of interesting indene and indanone derivatives.

Graphical abstract: Synthesis of silyl indenes by ruthenium-catalyzed aldehyde- and acylsilane-enabled C–H alkylation/cyclization

Supplementary files

Article information

Article type
Communication
Submitted
18 Oct 2023
Accepted
26 Nov 2023
First published
15 Dec 2023

Org. Biomol. Chem., 2024,22, 466-471

Synthesis of silyl indenes by ruthenium-catalyzed aldehyde- and acylsilane-enabled C–H alkylation/cyclization

T. Zhang, C. Zhang, X. Lu, C. Peng, Y. Zhang, X. Zhu, G. Zhong and J. Zhang, Org. Biomol. Chem., 2024, 22, 466 DOI: 10.1039/D3OB01699D

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