Enantioselective cyanosilylation of ketones by a catalytic double-activation method employing chiral Lewis acid and achiral N-oxide catalysts

	Enantioselective cyanosilylation of ketones by a catalytic double-activation method employing chiral Lewis acid and achiral N-oxide catalysts
	Chen, FX; Feng, XM; Qin, B; Zhang, GL; Jiang, YZ; Feng, XM, Sichuan Univ, Sichuan Key LGreen Chem & Technol, Coll Chem, Chengdu 610064, Peoples R China.
刊名	ORGANIC LETTERS
	2003
卷号	5 期号:6 页码:949_952
ISSN号	1523-7060
产权排序	4
英文摘要	Enantloselective addition of TMSCN to ketones is achieved by a catalytic double-activation method using 1a-Ti(IV) complex as the Lewis acid and achiral N-oxide 2 as the Lewis base to activate ketones and TMSCN, respectively.
学科主题	Chemistry, Organic
语种	英语
WOS记录号	WOS:000181586500043
公开日期	2011-07-08
内容类型	期刊论文
源URL	[http://210.75.237.14/handle/351003/17395]
专题	成都生物研究所_天然产物研究
通讯作者	Feng, XM, Sichuan Univ, Sichuan Key LGreen Chem & Technol, Coll Chem, Chengdu 610064, Peoples R China.
推荐引用方式 GB/T 7714	Chen, FX,Feng, XM,Qin, B,et al. Enantioselective cyanosilylation of ketones by a catalytic double-activation method employing chiral Lewis acid and achiral N-oxide catalysts[J]. ORGANIC LETTERS,2003,5(6):949_952.
APA	Chen, FX,Feng, XM,Qin, B,Zhang, GL,Jiang, YZ,&Feng, XM, Sichuan Univ, Sichuan Key LGreen Chem & Technol, Coll Chem, Chengdu 610064, Peoples R China..(2003).Enantioselective cyanosilylation of ketones by a catalytic double-activation method employing chiral Lewis acid and achiral N-oxide catalysts.ORGANIC LETTERS,5(6),949_952.
MLA	Chen, FX,et al."Enantioselective cyanosilylation of ketones by a catalytic double-activation method employing chiral Lewis acid and achiral N-oxide catalysts".ORGANIC LETTERS 5.6(2003):949_952.