This is the authors' abstract. We don't add key points for this paper.
An effective, green, mild, and metal‐free hypervalent iodine‐mediated approach for the synthesis of pyrroloquinolinediones from ortho‐carbonyl anilines and maleimides in a one‐pot manner at room temperature has been developed. This proposed protocol can synthesize biologically active pyrroloquinolinediones in a one‐pot manner utilizing readily available starting materials. This protocol generates H2O as the only by‐product during the reaction and shows a high atom economy. Operational simplicity, moderate reaction conditions, high atom economy, and high yield are some key features of this protocol.
Answers are grounded in this paper and cite their sources.
No takes yet. Share an insight, caveat, or question.
Alahmdi et al. (2024) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: