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Lewis acid assisted ring-closing metathesis of chiral diallylamines: An efficient approach to enantiopure pyrrolidine derivatives
Yang, Q; Xiao, WJ; Yu, ZK; Yu ZK(余正坤); Yu ZK(余正坤)
Source PublicationORGANIC LETTERS
2005-03-03
DOI10.1021/ol047356q
Volume7Issue:5Pages:871-874
Indexed BySCI ; IC ; CCR
SubtypeArticle
Department2
Funding Project203
Contribution Rank2;2
WOS HeadingsScience & Technology ; Physical Sciences
WOS SubjectChemistry, Organic
WOS Research AreaChemistry
WOS KeywordOLEFIN-METATHESIS ; TROPANE ALKALOIDS ; ENYNE METATHESIS ; NEW-GENERATION ; AMINO-ACIDS ; CATALYSTS ; HETEROCYCLES ; PHOSPHORUS ; PIPERIDINE ; COMPLEXES
AbstractLewis acid assisted ring-closing olefin metathesis (RCM) of chiral diallylamines, using the second generation RCM ruthenium-based catalyst, leads to enantiopure pyrrolidine derivatives in 79-93% yields under very mild conditions. The scope of the olefin metathesis has been expanded.
Language英语
URL查看原文
WOS IDWOS:000227313400031
Citation statistics
Cited Times:110[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://cas-ir.dicp.ac.cn/handle/321008/92545
Collection中国科学院大连化学物理研究所
Corresponding AuthorYu ZK(余正坤); Yu ZK(余正坤)
Affiliation1.Cent China Normal Univ, Coll Chem, Minist Educ, Key Lab Pesticide & Chem Biol, Wuhan 430079, Peoples R China
2.Chinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R China
Recommended Citation
GB/T 7714
Yang, Q,Xiao, WJ,Yu, ZK,et al. Lewis acid assisted ring-closing metathesis of chiral diallylamines: An efficient approach to enantiopure pyrrolidine derivatives[J]. ORGANIC LETTERS,2005,7(5):871-874.
APA Yang, Q,Xiao, WJ,Yu, ZK,余正坤,&余正坤.(2005).Lewis acid assisted ring-closing metathesis of chiral diallylamines: An efficient approach to enantiopure pyrrolidine derivatives.ORGANIC LETTERS,7(5),871-874.
MLA Yang, Q,et al."Lewis acid assisted ring-closing metathesis of chiral diallylamines: An efficient approach to enantiopure pyrrolidine derivatives".ORGANIC LETTERS 7.5(2005):871-874.
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