电邮这篇文章 Synthesis of Tetradecapentaenoic Acid Derivatives
- 作者: Kolodyazhnaya A.1, Kolodyazhny O.1
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隶属关系:
- V.P. Kukhar Institute of Bioorganic Chemistry and Petrochemistry of the National Academy of Sciences of Ukraine
- 期: 卷 89, 编号 10 (2019)
- 页面: 1998-2004
- 栏目: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/223106
- DOI: https://doi.org/10.1134/S1070363219100037
- ID: 223106
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详细
A 12-stage method for the stereoselective synthesis of tetradecapentaenoic acid derivatives using phosphoric reagents was developed. The key step in the synthesis is the Z-selective Wittig reaction between sorbaldehyde and triphenylphosphonium (6-methoxycarbonyl)hexanilide, as well as the Ramirez-Corey-Fuchs reaction and the Trost-Kazmaier rearrangement. The synthesized (2E,4E,8Z,10E,12E)-N-isobutyltetradeca-2,4,8,10,12-pentaenamide corresponds to a natural compound called γ-Sanshoöl.
作者简介
A. Kolodyazhnaya
V.P. Kukhar Institute of Bioorganic Chemistry and Petrochemistry of the National Academy of Sciences of Ukraine
Email: olegkol321@gmail.com
乌克兰, ul. Murmanskaya 1, Kiev, 02094
O. Kolodyazhny
V.P. Kukhar Institute of Bioorganic Chemistry and Petrochemistry of the National Academy of Sciences of Ukraine
编辑信件的主要联系方式.
Email: olegkol321@gmail.com
乌克兰, ul. Murmanskaya 1, Kiev, 02094
