应用天然产物 ›› 2016, Vol. 6 ›› Issue (2): 117-139.DOI: 10.1007/s13659-016-0092-8
Xianfu Shen, Yongyun Zhou, Yongkai Xi, Jingfeng Zhao, Hongbin Zhang
收稿日期:
2016-01-13
修回日期:
2016-02-19
出版日期:
2016-04-24
发布日期:
2018-02-08
通讯作者:
Hongbin Zhang,e-mail:zhanghb@ynu.edu.cn
基金资助:
Xianfu Shen, Yongyun Zhou, Yongkai Xi, Jingfeng Zhao, Hongbin Zhang
Received:
2016-01-13
Revised:
2016-02-19
Online:
2016-04-24
Published:
2018-02-08
Supported by:
摘要: In this paper, we report a full account of the synthesis of dimeric hexahydropyrroloindole alkaloids and its analogues. The key feature of our new strategy is the novel catalytic copper (10%) mediated intramolecular arylations of o-haloanilides followed by intermolecular oxidative dimerization of the resulting oxindoles in one pot. This sequential reaction leads to the key intermediates for the synthesis of (+)-chimonanthine, (+)-folicanthine, (-)-calycanthine and (-)-ditryptophenaline. Graphical Abstract In the presence of catalytic amount of cuprous iodide (10%), an intramolecular arylation of ohaloanilidesfollowedby an intermolecularoxidative dimerizationof the resultingoxindolesleads to a commonintermediatefor the synthesis of (+)-chimonanthine, (+)-folicanthine and (-)-calycanthine. Based on this cascade sequence, we also developed a flexible strategy towards the asymmetric syntheses of dimeric HPI alkaloids (-)-ditryptophenaline and its analogues.
Xianfu Shen, Yongyun Zhou, Yongkai Xi, Jingfeng Zhao, Hongbin Zhang. Total Synthesis of Dimeric HPI Alkaloids[J]. 应用天然产物, 2016, 6(2): 117-139.
Xianfu Shen, Yongyun Zhou, Yongkai Xi, Jingfeng Zhao, Hongbin Zhang. Total Synthesis of Dimeric HPI Alkaloids[J]. Natural Products and Bioprospecting, 2016, 6(2): 117-139.
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