CORC  > 南开大学
Asymmetric synthesis of spiro[chroman-3,3′-pyrazol] scaffolds with an all-carbon quaternary stereocenter via a oxa-Michael–Michael cascade strategy with bifunctional amine-thiourea organocatalysts
Weiping Zheng; Jiayong Zhang; Shuang Liu; Chengbin Yu; Zhiwei Miao
刊名RSC Advances
2015
卷号Vol.5 No.111页码:91108-91113
ISSN号2046-2069
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/1863490
专题南开大学
作者单位1.Collaborative Innovation Center of Chemical Science and Engineering , Tianjin 300071, People's Republic of China
2.a State Key Laboratory and Institute of Elemento-Organic Chemistry, Nankai University, Weijin Road 94, Tianjin 300071, People's Republic of China E-mail: miaozhiwei@nankai.edu.cn
推荐引用方式
GB/T 7714
Weiping Zheng,Jiayong Zhang,Shuang Liu,et al. Asymmetric synthesis of spiro[chroman-3,3′-pyrazol] scaffolds with an all-carbon quaternary stereocenter via a oxa-Michael–Michael cascade strategy with bifunctional amine-thiourea organocatalysts[J]. RSC Advances,2015,Vol.5 No.111:91108-91113.
APA Weiping Zheng,Jiayong Zhang,Shuang Liu,Chengbin Yu,&Zhiwei Miao.(2015).Asymmetric synthesis of spiro[chroman-3,3′-pyrazol] scaffolds with an all-carbon quaternary stereocenter via a oxa-Michael–Michael cascade strategy with bifunctional amine-thiourea organocatalysts.RSC Advances,Vol.5 No.111,91108-91113.
MLA Weiping Zheng,et al."Asymmetric synthesis of spiro[chroman-3,3′-pyrazol] scaffolds with an all-carbon quaternary stereocenter via a oxa-Michael–Michael cascade strategy with bifunctional amine-thiourea organocatalysts".RSC Advances Vol.5 No.111(2015):91108-91113.
个性服务
查看访问统计
相关权益政策
暂无数据
收藏/分享
所有评论 (0)
暂无评论
 

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。


©版权所有 ©2017 CSpace - Powered by CSpace