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Asymmetric [3+2] Cycloaddition of Olefins with Morita-Baylis-Hillman Carbonates Catalyzed by BINOL-Based Bifunctional Phosphine
Cui, Hai-Lei[1]; Tang, Xue[1,2]; Li, Meng-Fan[1]; Xu, Xing-Jie[1,3,4]; Shi, Yin[1]
2019
卷号30期号:7页码:845-850
URL标识查看原文
WOS记录号WOS:000466807700018
内容类型期刊论文
URI标识http://www.corc.org.cn/handle/1471x/4339245
专题成都中医药大学
作者单位1.[1]Chongqing Univ Arts & Sci, Lab Asymmetr Synth, 319 Honghe Ave, Chongqing 402160, Peoples R China
2.[2]Chengdu Univ Tradit Chinese Med, Sch Pharm, Chengdu 611137, Sichuan, Peoples R China
3.[3]Guangzhou Med Univ, Sch Pharmaceut Sci, Key Lab Mol Target & Clin Pharmacol, Guangzhou 511436, Guangdong, Peoples R China
4.[4]Guangzhou Med Univ, Affiliated Hosp 5, Guangzhou 511436, Guangdong, Peoples R China
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GB/T 7714
Cui, Hai-Lei[1],Tang, Xue[1,2],Li, Meng-Fan[1],et al. Asymmetric [3+2] Cycloaddition of Olefins with Morita-Baylis-Hillman Carbonates Catalyzed by BINOL-Based Bifunctional Phosphine[J],2019,30(7):845-850.
APA Cui, Hai-Lei[1],Tang, Xue[1,2],Li, Meng-Fan[1],Xu, Xing-Jie[1,3,4],&Shi, Yin[1].(2019).Asymmetric [3+2] Cycloaddition of Olefins with Morita-Baylis-Hillman Carbonates Catalyzed by BINOL-Based Bifunctional Phosphine.,30(7),845-850.
MLA Cui, Hai-Lei[1],et al."Asymmetric [3+2] Cycloaddition of Olefins with Morita-Baylis-Hillman Carbonates Catalyzed by BINOL-Based Bifunctional Phosphine".30.7(2019):845-850.
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