SmI2-mediated radical coupling strategy to Securinega alkaloids: total synthesis of (-)-14,15-dihydrosecurinine and formal total synthesis of (-)-securinine.

SmI2-mediated radical coupling strategy to Securinega alkaloids: total synthesis of (-)-14,15-dihydrosecurinine and formal total synthesis of (-)-securinine.
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SmI2介导的叶秋生物碱自由基偶联策略:(-)-14,15-二氢叶秋碱的全合成和(-)-叶秋碱的正式全合成。

DOI:
10.1021/jo502522x
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发表时间:
2015-01
影响因子:
3.6
通讯作者:
Huang Pei-Qiang
Huang Pei-Qiang
中科院分区:
化学2区
文献类型:
--
作者:
Zheng Xiao;Liu Juan;Ye Chen-Xi;Wang Ao;Wang Ai-E;Huang Pei-Qiang

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以一种易得的马来酰亚胺为原料,完成了(-)-14,15-二氢一次尿苷的不对称全合成和(-)-一次尿苷的形式全合成。一种简明的SMI2介导的自由基偶联策略被开发来构建
The asymmetric total synthesis of (-)-14,15-dihydrosecurinine and the formal total synthesis of (-)-securinine were accomplished starting from an easily available malimide. A concise SmI2-mediated radical coupling strategy has been developed to construct
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