摘要
Spiropyrazolone and tetrahydroxanthone are privileged heterocyclic architectures that are known for their diverse biological activities. Herein, we report a bifunctional squaramide-catalyzed [3 + 3] annulation approach for the asymmetric synthesis of spiropyrazolone-fused tetrahydroxanthone scaffolds from pyrazolinone and a chromone–indandione-derived 3C synthon. This integrated cascade reaction provided optically active scaffolds in moderate to excellent yields and enantioselectivities with excellent diastereoselectivity. Control experiments revealed mechanistic insights, and synthetic applications further highlighted the significance of this methodology.
| 原文 | 英語 |
|---|---|
| 頁(從 - 到) | 7349-7355 |
| 頁數 | 7 |
| 期刊 | Organic Letters |
| 卷 | 28 |
| 發行號 | 23 |
| DOIs | |
| 出版狀態 | 已發佈 - 2026 6月 12 |
ASJC Scopus subject areas
- 生物化學
- 物理與理論化學
- 有機化學
指紋
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