Phosphine-catalyzed asymmetric [4+1] annulation of activated alpha,beta-unsaturated ketones with Morita-Baylis-Hillman carbonates: enantioselective synthesis of spirooxindoles containing two adjacent quaternary stereocenters
Hu FL(胡方乐); Wei Y(魏音); Shi M(施敏)
刊名Chem. Commun.
2014
卷号50期号:64页码:8912-8914
其他题名膦催化的MBH产物和a,b-不饱和酮的[4+1]环加成反应, 高对映选择性地合成螺环氧化吲哚
通讯作者施敏
英文摘要The asymmetric [4+1] annulation of activated alpha,beta-unsaturated ketones with MBH carbonates catalyzed by bifunctional thiourea-phosphine catalysts derived from an axially chiral binaphthyl scaffold has been developed, giving spirooxindoles with two adjacent quaternary stereocenters in good yields with high enantioselectivities and moderate diastereoselectivities under mild conditions.
学科主题金属有机化学
收录类别SCI
原文出处http://dx.doi.org/10.1039/c4cc03479a
语种英语
内容类型期刊论文
源URL[http://ir.sioc.ac.cn/handle/331003/39080]  
专题上海有机化学研究所_金属有机化学国家重点实验室
作者单位中科院上海有机化学研究所
推荐引用方式
GB/T 7714
Hu FL,Wei Y,Shi M. Phosphine-catalyzed asymmetric [4+1] annulation of activated alpha,beta-unsaturated ketones with Morita-Baylis-Hillman carbonates: enantioselective synthesis of spirooxindoles containing two adjacent quaternary stereocenters[J]. Chem. Commun.,2014,50(64):8912-8914.
APA 胡方乐,魏音,&施敏.(2014).Phosphine-catalyzed asymmetric [4+1] annulation of activated alpha,beta-unsaturated ketones with Morita-Baylis-Hillman carbonates: enantioselective synthesis of spirooxindoles containing two adjacent quaternary stereocenters.Chem. Commun.,50(64),8912-8914.
MLA 胡方乐,et al."Phosphine-catalyzed asymmetric [4+1] annulation of activated alpha,beta-unsaturated ketones with Morita-Baylis-Hillman carbonates: enantioselective synthesis of spirooxindoles containing two adjacent quaternary stereocenters".Chem. Commun. 50.64(2014):8912-8914.
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