Issue 43, 2025

Synthesis of a pyrroloquinoline-containing polycyclic scaffold via decarboxylative [3+2] cycloaddition and aza-Wittig reactions

Abstract

A two-step reaction process involving decarboxylative [3+2] cycloaddition followed by the intramolecular aza-Wittig reaction is developed for making novel 5,5,6,6-fused polycyclic scaffold-containing pyrroloquinolines. The use of polymer-supported Ph3P in the aza-Wittig reaction simplified the removal of Ph3P(O) and reduced the loss of product during purification.

Graphical abstract: Synthesis of a pyrroloquinoline-containing polycyclic scaffold via decarboxylative [3+2] cycloaddition and aza-Wittig reactions

Supplementary files

Article information

Article type
Paper
Submitted
02 Aug 2025
Accepted
30 Sep 2025
First published
01 Oct 2025
This article is Open Access
Creative Commons BY license

New J. Chem., 2025,49, 18970-18973

Synthesis of a pyrroloquinoline-containing polycyclic scaffold via decarboxylative [3+2] cycloaddition and aza-Wittig reactions

L. Price, Z. Li and W. Zhang, New J. Chem., 2025, 49, 18970 DOI: 10.1039/D5NJ03128A

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