Highly enantioselective synthesis of alpha-fluoro-alpha-nitro esters via organocatalyzed asymmetric Michael addition
文献类型：期刊论文
| 作者 | Cui HF(崔海峰) ; Li P(李鹏) ; Wang XW(王晓伟) ; Chai Z(柴卓) ; Yang YQ(杨映权) ; Cai YP(蔡岳鹏) ; Zhu SZ(朱仕正) ; Zhao G(赵刚) |
| 刊名 | Tetrahedron
 |
| 出版日期 | 2011 |
| 卷号 | 67期号:2页码:312-317 |
| ISSN号 | 0040-4020 |
| 其他题名 | 用有机催化的不对称迈克尔加成反应高对映选择性的合成α-氟-α-硝基酯类化合物 |
| 通讯作者 | 朱仕正 ; 赵刚 |
| 英文摘要 | Primary amines catalyzed the asymmetric Michael addition of ethyl 2-fluoro-2-nitroacetate to enones to provide chiral alpha-fluoro-alpha-nitro ester ketones with two contiguous stereogenic centers, one of which is a fluorinated quaternary chiral center, with excellent enantioselectivities and in moderate to good yields. Crown Copyright (C) 2010 Published by Elsevier Ltd. All rights reserved. |
| 学科主题 | 有机氟化学 |
| 收录类别 | SCI |
| 原文出处 | http://dx.doi.org/10.1016/j.tet.2010.11.041 |
| 语种 | 英语 |
| WOS记录号 | WOS:000286499000005 |
| 公开日期 | 2013-01-18 |
| 源URL | [http://202.127.28.38/handle/331003/14512]  |
| 专题 | 上海有机化学研究所_中科院有机氟化学重点实验室 |
| 推荐引用方式 GB/T 7714 | Cui HF,Li P,Wang XW,et al. Highly enantioselective synthesis of alpha-fluoro-alpha-nitro esters via organocatalyzed asymmetric Michael addition[J]. Tetrahedron,2011,67(2):312-317. |
| APA | 崔海峰.,李鹏.,王晓伟.,柴卓.,杨映权.,...&赵刚.(2011).Highly enantioselective synthesis of alpha-fluoro-alpha-nitro esters via organocatalyzed asymmetric Michael addition.Tetrahedron,67(2),312-317. |
| MLA | 崔海峰,et al."Highly enantioselective synthesis of alpha-fluoro-alpha-nitro esters via organocatalyzed asymmetric Michael addition".Tetrahedron 67.2(2011):312-317. |
入库方式： OAI收割
来源：上海有机化学研究所
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