中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Aza-Baylis-Hillman reaction of N-tosylated imines with beta-substituted alpha,beta-unsaturated esters activated olefins; Lewis base

文献类型:期刊论文

作者Shi YL(时永灵) ; Shi M(施敏)
刊名Tetrahedron
出版日期2006
卷号62期号:2-3页码:461-475
其他题名磺酰亚胺和?-位取代的活化烯的aza-Baylis-Hillman反应
通讯作者施敏
英文摘要Aza-Baylis-Hillman reaction of N-tosylated imines with beta-substituted alpha,beta-unsaturated esters can take place under mild reaction conditions to give the corresponding Baylis-Hillman adducts in moderate to excellent Yields. (c) 2005 Elsevier Ltd. All rights reserved.
学科主题金属有机化学
收录类别SCI
原文出处http://dx.doi.org/10.1016/j.tet.2005.09.058
语种英语
公开日期2013-01-09
源URL[http://202.127.28.38/handle/331003/10060]  
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
Shi YL,Shi M. Aza-Baylis-Hillman reaction of N-tosylated imines with beta-substituted alpha,beta-unsaturated esters activated olefins; Lewis base[J]. Tetrahedron,2006,62(2-3):461-475.
APA Shi YL,&Shi M.(2006).Aza-Baylis-Hillman reaction of N-tosylated imines with beta-substituted alpha,beta-unsaturated esters activated olefins; Lewis base.Tetrahedron,62(2-3),461-475.
MLA Shi YL,et al."Aza-Baylis-Hillman reaction of N-tosylated imines with beta-substituted alpha,beta-unsaturated esters activated olefins; Lewis base".Tetrahedron 62.2-3(2006):461-475.

入库方式: OAI收割

来源:上海有机化学研究所

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