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Expeditious Entry to the Chamigrane Endoperoxide Family of Natural Products
Alternative Title过氧花柏烷类天然产物的简捷合成
Chen HJ(陈慧君); Wu YK(伍贻康)
2015
Source PublicationOrg. Lett.
Volume17Issue:3Pages:592-595
AbstractSeveral members of the recently reported peroxy chamigrane family of natural products were synthesized via a distereoselective route with a novel facial-selective epoxidation of a spiroundecadiene, a facile epoxide rearrangement, and a Co(II)-mediated silylperoxidation as the key steps. Adaptation of the diastereoselective route to an enantioselective one is also illustrated.
Subtype论文
Subject Area生命有机化学
DOI10.1021/ol503603t
URL查看原文
Indexed BySCI
Language英语
WOS IDWOS:000349274200051
Citation statistics
Cited Times:10[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.sioc.ac.cn/handle/331003/39484
Collection生命有机化学国家重点实验室
Corresponding AuthorWu YK(伍贻康)
Affiliation中科院上海有机化学研究所, 生命有机化学国家重点实验室
Recommended Citation
GB/T 7714
Chen HJ,Wu YK. Expeditious Entry to the Chamigrane Endoperoxide Family of Natural Products[J]. Org. Lett.,2015,17(3):592-595.
APA 陈慧君,&伍贻康.(2015).Expeditious Entry to the Chamigrane Endoperoxide Family of Natural Products.Org. Lett.,17(3),592-595.
MLA 陈慧君,et al."Expeditious Entry to the Chamigrane Endoperoxide Family of Natural Products".Org. Lett. 17.3(2015):592-595.
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