Total Synthesis of (-)-Geissoschizol through Ir-Catalyzed Allylic Amidation as the Key Step | |
Zheng, Yu1,2; Wei, Kun1; Yang, Yu-Rong1 | |
2017-12-01 | |
发表期刊 | ORGANIC LETTERS |
ISSN | 1523-7060 |
卷号 | 19期号:23页码:6460-6462 |
摘要 | The iridium-catalyzed, Zn(OTf)(2) promoted asymmetric allylic amidation of a secondary alcohol derived from tryptamine has been utilized to forge a tetrahydro-beta-carboline. Based on this key step, a novel, facile, and enantioselective total synthesis of (-)-geissoschizol was achieved in 10 steps. |
DOI | 10.1021/acs.orglett.7b03133 |
语种 | 英语 |
WOS记录号 | WOS:000417229000050 |
引用统计 | |
文献类型 | 期刊论文 |
条目标识符 | http://ir.kib.ac.cn/handle/151853/60618 |
专题 | 植物化学与西部植物资源持续利用国家重点实验室 |
作者单位 | 1.Chinese Acad Sci, Kunming Inst Bot, State Key Lab Phytochem & Plant Resources West Ch, Kunming 650201, Yunnan, Peoples R China 2.Univ Chinese Acad Sci, Beijing 100049, Peoples R China |
推荐引用方式 GB/T 7714 | Zheng, Yu,Wei, Kun,Yang, Yu-Rong. Total Synthesis of (-)-Geissoschizol through Ir-Catalyzed Allylic Amidation as the Key Step[J]. ORGANIC LETTERS,2017,19(23):6460-6462. |
APA | Zheng, Yu,Wei, Kun,&Yang, Yu-Rong.(2017).Total Synthesis of (-)-Geissoschizol through Ir-Catalyzed Allylic Amidation as the Key Step.ORGANIC LETTERS,19(23),6460-6462. |
MLA | Zheng, Yu,et al."Total Synthesis of (-)-Geissoschizol through Ir-Catalyzed Allylic Amidation as the Key Step".ORGANIC LETTERS 19.23(2017):6460-6462. |
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