中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Highly enantioselective Friedel–Crafts alkylation reaction catalyzed by rosin-derived tertiary amine–thiourea: synthesis of modified chromanes with anticancer potency

文献类型:期刊论文

作者Jiang XX(蒋先兴) ; Wu LP(吴立朋) ; Xing YH(邢燕红) ; Wang L(王龙) ; Wang SL(王守磊) ; Chen ZY(陈宗耀) ; Wang R(王锐)
刊名Chem. Commun.
出版日期2012
卷号48页码:446-448
ISSN号1359-7345
通讯作者王锐
中文摘要We present herein for the first time the synthesis and preliminary biological evaluation of various modified chromanes via a rosinderived tertiary amine–thiourea-catalyzed highly enantioselective Friedel–Crafts alkylation reaction.
学科主题物理化学
收录类别SCI
资助信息the National Natural Science Foundation of China (Nos. 20932003;90813012);the Key National S&T Program “Major New Drug Development” of the Ministry of Science and Technology of China (2009ZX09503-017);the Fundamental Research Funds for the Central Universities of China (860618)
语种英语
公开日期2013-10-11
源URL[http://210.77.64.217/handle/362003/3802]  
专题兰州化学物理研究所_OSSO国家重点实验室
推荐引用方式
GB/T 7714
Jiang XX,Wu LP,Xing YH,et al. Highly enantioselective Friedel–Crafts alkylation reaction catalyzed by rosin-derived tertiary amine–thiourea: synthesis of modified chromanes with anticancer potency[J]. Chem. Commun.,2012,48:446-448.
APA 蒋先兴.,吴立朋.,邢燕红.,王龙.,王守磊.,...&王锐.(2012).Highly enantioselective Friedel–Crafts alkylation reaction catalyzed by rosin-derived tertiary amine–thiourea: synthesis of modified chromanes with anticancer potency.Chem. Commun.,48,446-448.
MLA 蒋先兴,et al."Highly enantioselective Friedel–Crafts alkylation reaction catalyzed by rosin-derived tertiary amine–thiourea: synthesis of modified chromanes with anticancer potency".Chem. Commun. 48(2012):446-448.

入库方式: OAI收割

来源:兰州化学物理研究所

浏览0
下载0
收藏0
其他版本

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。