TransannularAcylation Facilitates C<sub>5</sub>–C<sub>9</sub> Bond Formationin Hyperforin Total Synthesis

Hyperforin is considered the flagship congener among polycyclic polyprenylated acylphloroglucinols due to its compelling and complex molecular architecture, coupled with remarkable biological activity, thus rendering it an appealing synthetic target for chemists over the past two decades. Herein, an innovative linear total synthesis of hyperforin is reported. Our synthesis relies on the formation of the bicyclo[3.3.1]nonane-2,4,9-trione framework via transannular acylation of a decorated eight-membered ring, followed by late stage bridgehead substitution.

Publication Details

Journal
Figshare
Published
2025-02-27
DOI
https://doi.org/10.1021/acs.orglett.5c00243.s001
Primary Topic
Natural Compound Pharmacology Studies
Type
article
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article

TransannularAcylation Facilitates C5–C9 Bond Formationin Hyperforin Total Synthesis

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Natural Compound Pharmacology Studies
article

TransannularAcylation Facilitates C5–C9 Bond Formationin Hyperforin Total Synthesis

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Abstract

Hyperforin is considered the flagship congener among polycyclic polyprenylated acylphloroglucinols due to its compelling and complex molecular architecture, coupled with remarkable biological activity, thus rendering it an appealing synthetic target for chemists over the past two decades. Herein, an innovative linear total synthesis of hyperforin is reported. Our synthesis relies on the formation of the bicyclo[3.3.1]nonane-2,4,9-trione framework via transannular acylation of a decorated eight-membered ring, followed by late stage bridgehead substitution.

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Openalex Percentile: Top 70%
Natural Compound Pharmacology Studies
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TransannularAcylation Facilitates C<sub>5</sub>–C<sub>9</sub> Bond Formationin Hyperforin Total Synthesis · Figshare (2025) | TGRS Research Map | TGRS