Synthesis of oxy-Functionalized Terpenoids involving the Hexahydroindane Skeleton as a Privileged Structure

Hexahydroindane scaffold can be found in the oxy-functionalized terpenoids such as cardiotonic steroids and picrotoxane sesquiterpenoids as a privileged structure for their biological activities. To clarify their novel functions, we have synthesized cardiotonic steroids, a pheromonal steroid, and picrotoxane sesquiterpenoid. In this publication, details of the synthetic studies on these naturally occurring products and related analogues are described, starting from tricyclic lactone as a new chiral building block.

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Publication Details

Journal
Journal of Synthetic Organic Chemistry Japan
Published
2024-09-01
DOI
https://doi.org/10.5059/yukigoseikyokaishi.82.877
Primary Topic
Synthetic Organic Chemistry Methods
Type
article
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article

Synthesis of oxy-Functionalized Terpenoids involving the Hexahydroindane Skeleton as a Privileged Structure

Atsuo Nakazaki
Journal of Synthetic Organic Chemistry Japan
Synthetic Organic Chemistry Methods
article

Synthesis of oxy-Functionalized Terpenoids involving the Hexahydroindane Skeleton as a Privileged Structure

Atsuo Nakazaki
article en

Abstract

Hexahydroindane scaffold can be found in the oxy-functionalized terpenoids such as cardiotonic steroids and picrotoxane sesquiterpenoids as a privileged structure for their biological activities. To clarify their novel functions, we have synthesized cardiotonic steroids, a pheromonal steroid, and picrotoxane sesquiterpenoid. In this publication, details of the synthetic studies on these naturally occurring products and related analogues are described, starting from tricyclic lactone as a new chiral building block.

Journal of Synthetic Organic Chemistry JapanVol. 82(9)
Iwate University (JP)
Openalex Percentile: Top 89%
Synthetic Organic Chemistry Methods
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