Pd(II)-Catalyzed C–H Activation/ O -Annulation toward Succinimide-Embedded Tetracyclic Pyranonaphthoquinones and Their Application as Metal Sensors

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Authors: Eswaran Kamaraj, Amrendra Kumar, Sonaimuthu Mohandoss, Raju S. Thombal, Y. H. Shin, Y. R. LEE
Cited by: 1
References: 103

Abstract

High Resolution Image Download MS PowerPoint Slide A Pd(II)-catalyzed cascade C–H activation/ O -annulation strategy is developed for the efficient synthesis of succinimide-integrated tetracyclic pyranonaphthoquinones using 3-aryl-2-hydroxy naphthoquinones with maleimides or itaconimides as substrates. This methodology provides a fast and efficient approach to prepare diverse tetracyclic pyranonaphthoquinones featuring spirosuccinimides or succinimide motifs via [5 + 1] cycloaddition. Notably, one of the synthesized compounds exhibited high sensitivity and selectivity as a fluorescent chemosensor for Fe 3+ ions, achieving a low detection limit of 30.07 × 10 –9 M.

Fields of Study & Subjects

Catalytic C–H Functionalization Methods Multicomponent Synthesis of Heterocycles Bioactive Compounds and Antitumor Agents

Publication details

Journal / source
ACS Omega
Publisher
American Chemical Society (ACS)
Volume
11
Issue
16
Pages
24822–24834
Publication date
14 April 2026
Language
EN