Biomimetic Synthesis of Myrtucommulones D–E

A concise and efficient biomimetic synthesis of myrtucommulones D-E has been achieved, proceeding in just 6-7 linear steps from readily available biogenetic building blocks. The key feature of the synthesis was the Zn-mediated skeletal rearrangement reaction, without the need for rare metal photocatalysts and visible light. Based on this biomimetic synthesis, four compounds demonstrated moderate to excellent cytotoxic activities against osteosarcoma cells (U2OS and 143B).

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-06-13
DOI
https://doi.org/10.1021/acs.joc.5c00859
Citations
3
Primary Topic
Synthesis of Organic Compounds
Type
article
Field-Weighted Citation Impact
4.18

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article

Biomimetic Synthesis of Myrtucommulones D–E

Yanxia Hu, Meiqi Zheng, Min-Jing Cheng, Wen‐Cai Ye et al.
3 citations
The Journal of Organic Chemistry
Synthesis of Organic Compounds
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article

Biomimetic Synthesis of Myrtucommulones D–E

Yanxia Hu, Meiqi Zheng, Min-Jing Cheng, Wen‐Cai Ye, Shi-Lin Lin, Chuang‐Chuang Li, Y. F. Zhu, Lei Wang, Sisi Wang, Ming-Fang Qi, Hong Min Guo, Yan-Yi Wu
article en
3 citations

Abstract

A concise and efficient biomimetic synthesis of myrtucommulones D-E has been achieved, proceeding in just 6-7 linear steps from readily available biogenetic building blocks. The key feature of the synthesis was the Zn-mediated skeletal rearrangement reaction, without the need for rare metal photocatalysts and visible light. Based on this biomimetic synthesis, four compounds demonstrated moderate to excellent cytotoxic activities against osteosarcoma cells (U2OS and 143B).

The Journal of Organic ChemistryVol. 90(25)
Southern University of Science and Technology (CN), Guangdong-Hongkong-Macau Joint Laboratory of Collaborative Innovation for Environmental Quality (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 6%
Synthesis of Organic Compounds
4.18
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