A practical route for the highly stereoselective synthesis of tetrasubstituted fluoroalkenes
文献类型：期刊论文
| 作者 | Cao CR(曹春如); Ou S(欧松); Jiang M(蒋敏); Liu JT(刘金涛) |
| 刊名 | Org. Biomol. Chem.
 |
| 出版日期 | 2014 |
| 卷号 | 12期号:3页码:467-473 |
| 其他题名 | 一种高选择性合成四取代含氟烯烃的实用方法 |
| 通讯作者 | 刘金涛 |
| 英文摘要 | A series of tetrasubstituted fluoroatkene derivatives were synthesized by the reaction of alpha-fluoro-beta-carbonyl benzothiazol-2-yl sulfones with various nucleophiles in good yields with high stereoselectivities. The predominant cis configuration of fluorine and alkynyl groups was observed. A single isomer was obtained when a ketone, acetate or amide was used as the substrate in the presence of a base. |
| 学科主题 | 氟化学 |
| 收录类别 | SCI |
| 原文出处 | http://dx.doi.org/10.1039/c3ob42093k |
| 语种 | 英语 |
| 源URL | [http://ir.sioc.ac.cn/handle/331003/38832]  |
| 专题 | 上海有机化学研究所_中科院有机氟化学重点实验室 |
| 作者单位 | 中科院上海有机化学研究所 |
| 推荐引用方式 GB/T 7714 | Cao CR,Ou S,Jiang M,et al. A practical route for the highly stereoselective synthesis of tetrasubstituted fluoroalkenes[J]. Org. Biomol. Chem.,2014,12(3):467-473. |
| APA | 曹春如,欧松,蒋敏,&刘金涛.(2014).A practical route for the highly stereoselective synthesis of tetrasubstituted fluoroalkenes.Org. Biomol. Chem.,12(3),467-473. |
| MLA | 曹春如,et al."A practical route for the highly stereoselective synthesis of tetrasubstituted fluoroalkenes".Org. Biomol. Chem. 12.3(2014):467-473. |
入库方式： OAI收割
来源：上海有机化学研究所
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