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Asymmetric Total Synthesis of (+)-21- epi -Eburnamonine Via a Photocatalytic Radical Cascade Reaction
Natural Products and Bioprospecting ( IF 4.8 ) Pub Date : 2020-11-05 , DOI: 10.1007/s13659-020-00276-8 Yuan Huang , Fanglin Xue , Hengmao Liu , Fei Xue , Xiao-Yu Liu , Hao Song , Yong Qin
中文翻译:
通过光催化自由基级联反应的不对称全合成(+)-21- Epi-Eburnamonine
更新日期:2020-11-06
Natural Products and Bioprospecting ( IF 4.8 ) Pub Date : 2020-11-05 , DOI: 10.1007/s13659-020-00276-8 Yuan Huang , Fanglin Xue , Hengmao Liu , Fei Xue , Xiao-Yu Liu , Hao Song , Yong Qin
An asymmetric total synthesis of (+)-21-epi-eburnamonine has been achieved. Key features of the synthesis include a visible-light photocatalytic intra-/intramolecular radical cascade reaction to assemble the tetracyclic ABCD ring system, and a highly diastereoselective Johnson-Claisen rearrangement to establish the C20 all-carbon quaternary stereocenter.
Graphic Abstract
中文翻译:
通过光催化自由基级联反应的不对称全合成(+)-21- Epi-Eburnamonine
已经实现了(+)-21- epi-金枪鱼碱的不对称全合成。合成的关键特征包括可见光光催化内/分子内自由基级联反应以组装四环ABCD环系统,以及高度非对映选择性的Johnson-Claisen重排以建立C20全碳四元立体中心。