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
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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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