A Concise Total Synthesis of (+)-Pedrolide

A concise total synthesis of (+)-pedrolide has been accomplished. Key steps include an intramolecular Diels-Alder reaction to rapidly construct the tetracyclic carbon skeleton from <i>(R)-</i>carvone and the late-stage application of two different MHAT reactions in advancing the highly functionalized carane moiety.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2025-12-22
DOI
https://doi.org/10.1021/jacs.5c17555
Citations
1
Primary Topic
Synthetic Organic Chemistry Methods
Type
article
Field-Weighted Citation Impact
0.94
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article

A Concise Total Synthesis of (+)-Pedrolide

John L. Wood, Yushang Zhou, Hao Shen
1 citations
Journal of the American Chemical Society
Synthetic Organic Chemistry Methods
0.94
article

A Concise Total Synthesis of (+)-Pedrolide

John L. Wood, Yushang Zhou, Hao Shen
article en
1 citations

Abstract

A concise total synthesis of (+)-pedrolide has been accomplished. Key steps include an intramolecular Diels-Alder reaction to rapidly construct the tetracyclic carbon skeleton from <i>(R)-</i>carvone and the late-stage application of two different MHAT reactions in advancing the highly functionalized carane moiety.

Journal of the American Chemical SocietyVol. 148(1)
Baylor University (US)
Openalex Percentile: Top 19%
Synthetic Organic Chemistry Methods
0.94
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