QQ客服 官方微博 反馈留言

	Rational Design of Sterically and Electronically Easily Tunable Chiral Bisimidazolines and Their Applications in Dual Lewis Acid/Broensted Base Catalysis for Highly Enantioselective Nitroaldol (Henry) Reactions.
	Kuoyan Ma; Jingsong You
刊名	ChemInform
	2007
卷号	Vol.38 No.23
关键词	nitro alcohols nitro compounds (benzene compounds) diastereoselective syntheses, enantioselective syntheses (incl. cis/trans-isomerism)
ISSN号	1522-2667
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/1997284
专题	四川大学
作者单位	Key Lab. Green Chem. Technol., Sichuan Univ., Chengdu, Sichuan 610064, Peop. Rep. China
推荐引用方式 GB/T 7714	Kuoyan Ma,Jingsong You. Rational Design of Sterically and Electronically Easily Tunable Chiral Bisimidazolines and Their Applications in Dual Lewis Acid/Broensted Base Catalysis for Highly Enantioselective Nitroaldol (Henry) Reactions.[J]. ChemInform,2007,Vol.38 No.23.
APA	Kuoyan Ma,&Jingsong You.(2007).Rational Design of Sterically and Electronically Easily Tunable Chiral Bisimidazolines and Their Applications in Dual Lewis Acid/Broensted Base Catalysis for Highly Enantioselective Nitroaldol (Henry) Reactions..ChemInform,Vol.38 No.23.
MLA	Kuoyan Ma,et al."Rational Design of Sterically and Electronically Easily Tunable Chiral Bisimidazolines and Their Applications in Dual Lewis Acid/Broensted Base Catalysis for Highly Enantioselective Nitroaldol (Henry) Reactions.".ChemInform Vol.38 No.23(2007).

个性服务

查看访问统计

相关权益政策

暂无数据

收藏/分享

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。