Gold-catalyzed multicomponent synthesis of aminoindolizines from aldehydes, amines, and Alkynes under solvent-free conditions or in water
Yan B(闫彬) ; Liu YH(刘元红)
刊名Org. Lett.
2007
卷号9期号:21页码:4323-4326
ISSN号1523-7060
其他题名金催化的在水相以及无溶剂条件下的醛、胺及炔烃的多组分反应研究:氨基取代的中氮茚的合成
通讯作者刘元红
英文摘要A goid(III)-catalyzed multicomponent coupling/cycloisomerization reaction of heteroaryl aldehydes, amines, and alkynes under solvent-free conditions or in water has been developed. This methodology provides rapid access to substituted aminoindolizines with high atom economy and high catalytic efficiency. Especially, the coupling of enantiomerically enriched amino acid derivatives produces the corresponding N-indolizine-incorporated amino acid derivatives without loss of enantiomeric purity.
学科主题金属有机化学
收录类别SCI
原文出处http://dx.doi.org/10.1021/o1701886e
语种英语
WOS记录号WOS:000249987200060
公开日期2013-03-11
内容类型期刊论文
源URL[http://202.127.28.38/handle/331003/24241]  
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
Yan B,Liu YH. Gold-catalyzed multicomponent synthesis of aminoindolizines from aldehydes, amines, and Alkynes under solvent-free conditions or in water[J]. Org. Lett.,2007,9(21):4323-4326.
APA 闫彬,&刘元红.(2007).Gold-catalyzed multicomponent synthesis of aminoindolizines from aldehydes, amines, and Alkynes under solvent-free conditions or in water.Org. Lett.,9(21),4323-4326.
MLA 闫彬,et al."Gold-catalyzed multicomponent synthesis of aminoindolizines from aldehydes, amines, and Alkynes under solvent-free conditions or in water".Org. Lett. 9.21(2007):4323-4326.
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