Synthesis of a Functionalized Bicyclo[3.2.1]Octane: A Common Subunit to Kauranes, Grayananes, and Gibberellanes

Kauranes, grayananes, and gibberellanes are three important diterpenoid families. These natural products all share a bicyclo[3.2.1]octane skeleton, with oxidation at very specific positions. In this manuscript, we describe the synthesis of a bicyclo[3.2.1]octane building block, which could serve as a potential intermediate for the synthesis of natural products from these three families. A first approach relying on a 1,4-sila-Prins cyclization was first explored, which required the selective functionalization of dihydrocarvone (via C─H activation and selective oxidation). This strategy resulted in a dead end when a 1,2-cyclization product was obtained. An alternative strategy relying on ring-closing metathesis (RCM) allowed to successfully achieve the synthesis of the desired scaffold in 8 steps from cyclohexenone.

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Journal
Chemistry - A European Journal
Published
2025-09-13
DOI
https://doi.org/10.1002/chem.202502441
Primary Topic
Bioactive Natural Diterpenoids Research
Type
article
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article

Synthesis of a Functionalized Bicyclo[3.2.1]Octane: A Common Subunit to Kauranes, Grayananes, and Gibberellanes

Aurélien de la Torre, Cyrille Kouklovsky, Nicolas Fay, Camil Benbouziyane
Chemistry - A European Journal
Bioactive Natural Diterpenoids Research
article

Synthesis of a Functionalized Bicyclo[3.2.1]Octane: A Common Subunit to Kauranes, Grayananes, and Gibberellanes

Aurélien de la Torre, Cyrille Kouklovsky, Nicolas Fay, Camil Benbouziyane
article en

Abstract

Kauranes, grayananes, and gibberellanes are three important diterpenoid families. These natural products all share a bicyclo[3.2.1]octane skeleton, with oxidation at very specific positions. In this manuscript, we describe the synthesis of a bicyclo[3.2.1]octane building block, which could serve as a potential intermediate for the synthesis of natural products from these three families. A first approach relying on a 1,4-sila-Prins cyclization was first explored, which required the selective functionalization of dihydrocarvone (via C─H activation and selective oxidation). This strategy resulted in a dead end when a 1,2-cyclization product was obtained. An alternative strategy relying on ring-closing metathesis (RCM) allowed to successfully achieve the synthesis of the desired scaffold in 8 steps from cyclohexenone.

Chemistry - A European JournalVol. 31(64)
Centre National de la Recherche Scientifique (FR), Institut de Chimie Moléculaire et des Matériaux d'Orsay (FR)
Openalex Percentile: Top 78%
Bioactive Natural Diterpenoids Research
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