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N-Alkylation of Indole via Ring-Closing Metathesis/Isomerization/Mannich Cascade under Ruthenium/Chiral Phosphoric Acid Sequential Catalysis
Alternative Title通过钌/手性磷酸串联催化的关环烯烃复分解/异构化/Mannich反应实现吲哚的N-烷基化
Shi YC(石延超); Wang SG(王守国); Yin Q(殷勤); You SL(游书力)
2014
Source PublicationOrg. Chem. Front.
Volume1Pages:39-43
AbstractA sequential catalysis by combining the Zhan-1B catalyst with chiral phosphoric acid has been utilized for N-alkylation of indole through a ring-closing metathesis/double bond isomerization/Mannich reaction cascade. Enantioenriched γ-lactams were synthesized in up to 92% yield and 95% ee.
Subject Area金属有机化学
DOI10.1039/c3qo00008g
URL查看原文
Language英语
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Document Type期刊论文
Identifierhttp://ir.sioc.ac.cn/handle/331003/39037
Collection金属有机化学国家重点实验室
Corresponding AuthorYou SL(游书力)
Affiliation中科院上海有机化学研究所
Recommended Citation
GB/T 7714
Shi YC,Wang SG,Yin Q,et al. N-Alkylation of Indole via Ring-Closing Metathesis/Isomerization/Mannich Cascade under Ruthenium/Chiral Phosphoric Acid Sequential Catalysis[J]. Org. Chem. Front.,2014,1:39-43.
APA 石延超,王守国,殷勤,&游书力.(2014).N-Alkylation of Indole via Ring-Closing Metathesis/Isomerization/Mannich Cascade under Ruthenium/Chiral Phosphoric Acid Sequential Catalysis.Org. Chem. Front.,1,39-43.
MLA 石延超,et al."N-Alkylation of Indole via Ring-Closing Metathesis/Isomerization/Mannich Cascade under Ruthenium/Chiral Phosphoric Acid Sequential Catalysis".Org. Chem. Front. 1(2014):39-43.
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