Total Synthesis of Berkeleyone A and Preaustinoid A through Epoxypolyene Cyclization

A bioinspired Lewis acid-catalyzed epoxypolyene cyclization was developed to construct the tetracyclic framework containing a bicyclo[3.3.1]nonane core and seven chiral centers. The usage of this approach for assembling these natural products of 6/6/6/6 tetracyclic skeleton with bicyclo[3.3.1]nonane core is demonstrated by the total synthesis of highly oxidized berkeleyone A and preaustinoid A.

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Publication Details

Journal
Angewandte Chemie International Edition
Published
2024-10-24
DOI
https://doi.org/10.1002/anie.202416211
Citations
8
Primary Topic
Synthetic Organic Chemistry Methods
Type
article
Field-Weighted Citation Impact
2.00

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article

Total Synthesis of Berkeleyone A and Preaustinoid A through Epoxypolyene Cyclization

Shengfu Duan, Zhe‐Ran Chang, Zhixiang Xie, Xingyi Li
8 citations
Angewandte Chemie International Edition
Synthetic Organic Chemistry Methods
2.00
article

Total Synthesis of Berkeleyone A and Preaustinoid A through Epoxypolyene Cyclization

Shengfu Duan, Zhe‐Ran Chang, Zhixiang Xie, Xingyi Li
article en
8 citations

Abstract

A bioinspired Lewis acid-catalyzed epoxypolyene cyclization was developed to construct the tetracyclic framework containing a bicyclo[3.3.1]nonane core and seven chiral centers. The usage of this approach for assembling these natural products of 6/6/6/6 tetracyclic skeleton with bicyclo[3.3.1]nonane core is demonstrated by the total synthesis of highly oxidized berkeleyone A and preaustinoid A.

Angewandte Chemie International EditionVol. 64(4)
State Key Laboratory of Applied Organic Chemistry, Lanzhou University (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 14%
Synthetic Organic Chemistry Methods
2.00
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