A new and efficient asymmetric synthesis of 1-amino-1-alkylphosphonic acids

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	A new and efficient asymmetric synthesis of 1-amino-1-alkylphosphonic acids
	Yuan CY(袁承业) ; Li SS(李树森) ; Wang GQ(王国权)
刊名	Heteroatom Chem.
	2000
卷号	11 期号:7 页码:528-535
ISSN号	1042-7163
其他题名	不对称合成α-氨基膦酸的新方法
英文摘要	A new and efficient method for the asymmetric synthesis of 1-amino-1-alkyl phosphonic acids is described. It involves a diastereoselective alkylation of a bicyclic chloromethyl phosphonamide derived from (S)-2-anilinomethylpyrrolidine, with subsequent conversions leading to an amino compound by the staudinger method. Acid hydrolysis affords the target molecule of high enantiomeric purity and good yield.
学科主题	元素有机化学
收录类别	SCI
原文出处	http://dx.doi.org/10.1002/1098-1071(2000)11:7<528::AID-HC11>3.0.CO;2-W
语种	英语
WOS记录号	WOS:000165651800010
公开日期	2013-01-09
内容类型	期刊论文
源URL	[http://202.127.28.38/handle/331003/10984]
专题	上海有机化学研究所_上海有机化学研究所
推荐引用方式 GB/T 7714	Yuan CY,Li SS,Wang GQ. A new and efficient asymmetric synthesis of 1-amino-1-alkylphosphonic acids[J]. Heteroatom Chem.,2000,11(7):528-535.
APA	袁承业,李树森,&王国权.(2000).A new and efficient asymmetric synthesis of 1-amino-1-alkylphosphonic acids.Heteroatom Chem.,11(7),528-535.
MLA	袁承业,et al."A new and efficient asymmetric synthesis of 1-amino-1-alkylphosphonic acids".Heteroatom Chem. 11.7(2000):528-535.