Highly enantioselective reduction of ketones by chiral diol-modified lithium aluminum hydride reagents

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	Highly enantioselective reduction of ketones by chiral diol-modified lithium aluminum hydride reagents
	Sun KP(孙鲲鹏)
刊名	Tetrahedron Letters
	2006
卷号	47 期号:4 页码:463-465
关键词	asymmetric reduction ketone diol lithium tetrahydridoaluminate
ISSN号	0040-4039
通讯作者	徐贤伦
中文摘要	Some readily available chiral diols from indene and (D)-mannitol were investigated as chiral modifiers in lithium aluminum hydride reduction of ketones, and it was discovered that further modification of these reducing reagents by a simple a-amino alcohol resulted in a remarkable increase in optical yield. Among the investigated chiral modifiers, chiral diol I gave the highest enantio selectivities.
学科主题	物理化学
收录类别	SCI
资助信息	National Nature Science Foundation of China (No. 29933050)
语种	英语
WOS记录号	WOS:000234624600013
公开日期	2013-08-27
内容类型	期刊论文
源URL	[http://210.77.64.217/handle/362003/3684]
专题	兰州化学物理研究所_绿色化学研究发展中心
推荐引用方式 GB/T 7714	Sun KP. Highly enantioselective reduction of ketones by chiral diol-modified lithium aluminum hydride reagents[J]. Tetrahedron Letters,2006,47(4):463-465.
APA	孙鲲鹏.(2006).Highly enantioselective reduction of ketones by chiral diol-modified lithium aluminum hydride reagents.Tetrahedron Letters,47(4),463-465.
MLA	孙鲲鹏."Highly enantioselective reduction of ketones by chiral diol-modified lithium aluminum hydride reagents".Tetrahedron Letters 47.4(2006):463-465.