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June 3, 2026Organic Letters0 citations

Organocatalytic 3 + 3 Annulation of Pyrazolinone and Chromone–Indandione Derivatives: Access to Spiropyrazolone-Fused Tetrahydroxanthones

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GKGanesh Shantaram KhomaneWWWei-Chi WuCCChia-Yen Chang

Key Points

  • This research aims to develop an efficient method for synthesizing spiropyrazolone-fused tetrahydroxanthones.
  • Bifunctional squaramide-catalyzed [3 + 3] annulation reaction
  • Utilization of pyrazolinone and chromone-indandione-derived 3C synthons
  • Evaluation of optical activity, yields, and selectivity in synthesized compounds.
  • Optically active compounds were obtained in moderate to excellent yields
  • Enantiomeric excesses demonstrated excellent enantioselectivity
  • Control experiments provided insights into the reaction mechanism.

Abstract

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.

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Cite This Study

Khomane et al. (2026) studied this question.

synapsesocial.com/papers/6a1fc616dee9eb8c0dce7603https://doi.org/10.1021/acs.orglett.6c01712
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