Highly Enantioselective Friedel-Crafts Reaction of 4,7-Dihydroindoles with beta,gamma-Unsaturated alpha-Keto Esters by Chiral Bronsted Acids
文献类型：期刊论文
| 作者 | Ceng M(曾蜜) ; Kang Q(康强) ; He QL(贺庆利) ; You SL(游书力) |
| 刊名 | Adv. Synth. Catal.
 |
| 出版日期 | 2008 |
| 卷号 | 350期号:14-15页码:2169-2173 |
| ISSN号 | 1615-4150 |
| 其他题名 | Highly Enantioselective Friedel-Crafts Reaction of 4,7-Dihydroindoles with beta,gamma-Unsaturated alpha-Keto Esters by Chiral Bronsted Acids |
| 通讯作者 | 游书力 |
| 英文摘要 | A highly efficient Friedel-Crafts reaction of 4,7-dihydroindoles with beta,gamma-unsaturated alpha-keto esters by a chiral N-triflyl phosphoramide was realized, affording the 2-substituted 4,7-dihydroindoles with up to 98% ee for a wide range of substrates. The Friedel-Crafts alkylation together with a subsequent oxidation of the product with p-benzoquinone led to a 2-alkylated indole derivative in 98% ee. |
| 学科主题 | 金属有机化学 |
| 收录类别 | SCI |
| 原文出处 | http://dx.doi.org/10.1002/adsc.200800523 |
| 语种 | 英语 |
| WOS记录号 | WOS:000260760700002 |
| 公开日期 | 2013-03-04 |
| 源URL | [http://202.127.28.38/handle/331003/22472]  |
| 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 | Ceng M,Kang Q,He QL,et al. Highly Enantioselective Friedel-Crafts Reaction of 4,7-Dihydroindoles with beta,gamma-Unsaturated alpha-Keto Esters by Chiral Bronsted Acids[J]. Adv. Synth. Catal.,2008,350(14-15):2169-2173. |
| APA | 曾蜜,康强,贺庆利,&游书力.(2008).Highly Enantioselective Friedel-Crafts Reaction of 4,7-Dihydroindoles with beta,gamma-Unsaturated alpha-Keto Esters by Chiral Bronsted Acids.Adv. Synth. Catal.,350(14-15),2169-2173. |
| MLA | 曾蜜,et al."Highly Enantioselective Friedel-Crafts Reaction of 4,7-Dihydroindoles with beta,gamma-Unsaturated alpha-Keto Esters by Chiral Bronsted Acids".Adv. Synth. Catal. 350.14-15(2008):2169-2173. |
入库方式： OAI收割
来源：上海有机化学研究所
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