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	Organocatalytic tandem Morita-Baylis-Hillman-Michael reaction for asymmetric synthesis of a drug-like oxa-spirocyclic indanone scaffold.
	Li, X; Yang, L; Peng, C; Xie, X; Leng, HJ; Wang, B; Tang, ZW; He, G; Ouyang, L; Huang, W
刊名	Chemical Communications
	2013
卷号	Vol.49 No.77页码:8692-8694
ISSN号	1359-7345;1364-548X
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/1841928
专题	四川大学
作者单位	1.Chengdu Univ Tradit Chinese Med, State Key Lab Breeding Base Systemat Res Dev & Ut, Chengdu 611137, Peoples R China 2.Sichuan Univ, West China Hosp, State Key Lab Biotherapy, Chengdu 610041, Peoples R China 3.Chengdu Univ Tradit Chinese Med, Sch Pharm, Chengdu 611137, Peoples R China
推荐引用方式 GB/T 7714	Li, X,Yang, L,Peng, C,et al. Organocatalytic tandem Morita-Baylis-Hillman-Michael reaction for asymmetric synthesis of a drug-like oxa-spirocyclic indanone scaffold.[J]. Chemical Communications,2013,Vol.49 No.77:8692-8694.
APA	Li, X.,Yang, L.,Peng, C.,Xie, X.,Leng, HJ.,...&Huang, W.(2013).Organocatalytic tandem Morita-Baylis-Hillman-Michael reaction for asymmetric synthesis of a drug-like oxa-spirocyclic indanone scaffold..Chemical Communications,Vol.49 No.77,8692-8694.
MLA	Li, X,et al."Organocatalytic tandem Morita-Baylis-Hillman-Michael reaction for asymmetric synthesis of a drug-like oxa-spirocyclic indanone scaffold.".Chemical Communications Vol.49 No.77(2013):8692-8694.

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