Total Synthesis of (+)-Niduenes A and B

Niduenes A and B, two tetraquinane sesterterpenoids, possess a complex and intriguing 5/5/5/5/6 pentacyclic skeleton with eight contiguous stereocenters. We have achieved the first total synthesis of niduenes A and B in 16 and 14 steps, respectively. The synthesis features a Pauson-Khand reaction to generate the 5/5 bicycle, a Pd-catalyzed oxidative cyclization to construct the congested triquinane framework, and a radical cyclization to assemble the tetraquinane skeleton.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2026-06-25
DOI
https://doi.org/10.1021/jacs.6c08709
Primary Topic
Synthetic Organic Chemistry Methods
Type
article
Field-Weighted Citation Impact
0.00

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article

Total Synthesis of (+)-Niduenes A and B

Yanxing Jia, Chuanzhen Tan, H Lin, Yuan Wang
Journal of the American Chemical Society
Synthetic Organic Chemistry Methods
article

Total Synthesis of (+)-Niduenes A and B

Yanxing Jia, Chuanzhen Tan, H Lin, Yuan Wang
article en

Abstract

Niduenes A and B, two tetraquinane sesterterpenoids, possess a complex and intriguing 5/5/5/5/6 pentacyclic skeleton with eight contiguous stereocenters. We have achieved the first total synthesis of niduenes A and B in 16 and 14 steps, respectively. The synthesis features a Pauson-Khand reaction to generate the 5/5 bicycle, a Pd-catalyzed oxidative cyclization to construct the congested triquinane framework, and a radical cyclization to assemble the tetraquinane skeleton.

Journal of the American Chemical Society
Peking University (CN), State Key Laboratory of Natural and Biomimetic Drugs (CN)
National Natural Science Foundation of China, National Outstanding Youth Science Fund Project of National Natural Science Foundation of China
Openalex Percentile: Top 13%
Synthetic Organic Chemistry Methods
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