Kobayashi’sAryne Precursor for the One-StepSynthesis of Anthraquinones and Its Application to the Total Synthesisof Chrysophanol, Danthron, and Physcion

A one-step synthetic method to access medicinally essential anthraquinones has been developed by reacting Kobayashi’s aryne precursors with 3-sulfonylphthalides following [4 + 2] Hauser–Kraus annulation reaction. The developed method has been implemented for the total synthesis of bioactive natural products, chrysophanol, danthron, and physcion in 30, 20, and 36% overall yields, respectively, from known compounds.

Publication Details

Journal
Figshare
Published
2025-02-06
DOI
https://doi.org/10.1021/acs.joc.4c03041.s001
Primary Topic
Cyclization and Aryne Chemistry
Type
article
Field-Weighted Citation Impact
0.00
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article

Kobayashi’sAryne Precursor for the One-StepSynthesis of Anthraquinones and Its Application to the Total Synthesisof Chrysophanol, Danthron, and Physcion

Figshare
Cyclization and Aryne Chemistry
article

Kobayashi’sAryne Precursor for the One-StepSynthesis of Anthraquinones and Its Application to the Total Synthesisof Chrysophanol, Danthron, and Physcion

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Abstract

A one-step synthetic method to access medicinally essential anthraquinones has been developed by reacting Kobayashi’s aryne precursors with 3-sulfonylphthalides following [4 + 2] Hauser–Kraus annulation reaction. The developed method has been implemented for the total synthesis of bioactive natural products, chrysophanol, danthron, and physcion in 30, 20, and 36% overall yields, respectively, from known compounds.

Figshare
Openalex Percentile: Top 63%
Cyclization and Aryne Chemistry
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