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	Mechanism, selectivity, and reactivity of iridium- and rhodium-catalyzed intermolecular ketone alpha-alkylation with unactivated olefins via an enamide directing strategy
	Li, X.a; Wu, H.a; Lang, Y.a; Huang, G.a,b
刊名	Catalysis science & technology
	2018
卷号	Vol.8 No.9页码:2417-2426
ISSN号	2044-4753
URL标识	查看原文
内容类型	期刊论文
URI标识	http://www.corc.org.cn/handle/1471x/2895408
专题	天津大学
作者单位	1.aDepartment of Chemistry, School of Science and Tianjin, Key Laboratory of Molecular Optoelectronic Sciences, Tianjin University, Tianjin, 300072, China 2.bNational Demonstration Center for Experimental Chemistry and Chemical Engineering Education, Natl. Virtual Simulat. Experimental Teaching Center for Chemistry and Chemical Engineering Education, Tianjin University, Tianjin, 300072, China
推荐引用方式 GB/T 7714	Li, X.a,Wu, H.a,Lang, Y.a,et al. Mechanism, selectivity, and reactivity of iridium- and rhodium-catalyzed intermolecular ketone alpha-alkylation with unactivated olefins via an enamide directing strategy[J]. Catalysis science & technology,2018,Vol.8 No.9:2417-2426.
APA	Li, X.a,Wu, H.a,Lang, Y.a,&Huang, G.a,b.(2018).Mechanism, selectivity, and reactivity of iridium- and rhodium-catalyzed intermolecular ketone alpha-alkylation with unactivated olefins via an enamide directing strategy.Catalysis science & technology,Vol.8 No.9,2417-2426.
MLA	Li, X.a,et al."Mechanism, selectivity, and reactivity of iridium- and rhodium-catalyzed intermolecular ketone alpha-alkylation with unactivated olefins via an enamide directing strategy".Catalysis science & technology Vol.8 No.9(2018):2417-2426.

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