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Total Synthesis of Hapalindole-Type Natural Products
Alternative TitleTotal Synthesis of Hapalindole-Type Natural Products
Lu ZH(陆钊洪); Yang M(阳铭); Chen PX(陈鹏西); Xiong XC(熊小春); Li A(李昂)
2014
Source PublicationAngew. Chem.-Int. Edit.
Volume53Issue:50Pages:13840-13844
AbstractA unified and bioinspired oxidative cyclization strategy was used in the first total syntheses of naturally occurring 12-epi-hapalindoleQ isonitrile, hapalonamideH, deschloro 12-epi-fischerindoleI nitrile, and deschloro 12-epi-fischerindoleW nitrile, as well as the structural revision of the latter. HapalindolesH and Q were also synthesized.
Subject Area生命有机化学
DOI10.1002/anie.201406626
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Indexed BySCI
Language英语
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Document Type期刊论文
Identifierhttp://ir.sioc.ac.cn/handle/331003/38965
Collection生命有机化学国家重点实验室
Corresponding AuthorLi A(李昂)
Affiliation中科院上海有机化学研究所
Recommended Citation
GB/T 7714
Lu ZH,Yang M,Chen PX,et al. Total Synthesis of Hapalindole-Type Natural Products[J]. Angew. Chem.-Int. Edit.,2014,53(50):13840-13844.
APA 陆钊洪,阳铭,陈鹏西,熊小春,&李昂.(2014).Total Synthesis of Hapalindole-Type Natural Products.Angew. Chem.-Int. Edit.,53(50),13840-13844.
MLA 陆钊洪,et al."Total Synthesis of Hapalindole-Type Natural Products".Angew. Chem.-Int. Edit. 53.50(2014):13840-13844.
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