tert-Butyldimethylsilyl-Directed Highly Enantioselective Approach to Axially Chiral alpha-Allenols

	tert-Butyldimethylsilyl-Directed Highly Enantioselective Approach to Axially Chiral alpha-Allenols
	Ye JT(叶俊涛) ; Fan W(范武) ; Ma SM(麻生明)
刊名	Chem.-Eur. J.
	2013
卷号	19 期号:2 页码:716-720
ISSN号	0947-6539
其他题名	叔丁基二甲基氯硅基导向的高对映选择性合成轴手性α-联烯醇的方法
通讯作者	麻生明
英文摘要	A highly efficient and enantioselective synthesis of axially chiral alpha-allenols was realized in practical yields with 96-99% ee or de from TBS-protected propargylic alcohols, aldehydes, and a commercially available, inexpensive, chiral, secondary amine
学科主题	金属有机化学
收录类别	SCI
原文出处	http://dx.doi.org/10.1002/chem.201201948
语种	英语
WOS记录号	WOS:000313161200035
公开日期	2014-10-16
内容类型	期刊论文
源URL	[http://ir.sioc.ac.cn/handle/331003/29454]
专题	上海有机化学研究所_金属有机化学国家重点实验室
推荐引用方式 GB/T 7714	Ye JT,Fan W,Ma SM. tert-Butyldimethylsilyl-Directed Highly Enantioselective Approach to Axially Chiral alpha-Allenols[J]. Chem.-Eur. J.,2013,19(2):716-720.
APA	叶俊涛,范武,&麻生明.(2013).tert-Butyldimethylsilyl-Directed Highly Enantioselective Approach to Axially Chiral alpha-Allenols.Chem.-Eur. J.,19(2),716-720.
MLA	叶俊涛,et al."tert-Butyldimethylsilyl-Directed Highly Enantioselective Approach to Axially Chiral alpha-Allenols".Chem.-Eur. J. 19.2(2013):716-720.