Reagent-controlled asymmetric iodolactonization using cinchona alkaloids as chiral sources
文献类型：期刊论文
| 作者 | Wang M ; Gao LX ; Yue W ; Mai WP |
| 刊名 | synthetic communications
 |
| 出版日期 | 2004 |
| 卷号 | 34期号:6页码:1023-1032 |
| 关键词 | AUXILIARY 3 HALOCYCLIZATION AMIDES 5-DISUBSTITUTED-GAMMA-BUTYROLACTONES |
| ISSN号 | 0039-7911 |
| 通讯作者 | gao lx |
| 中文摘要 | a novel method for reagent-controlled asymmetric iodolactonization of 5-aryl-4-pentenoic acids is reported. this work uses carboxylate ion pairs combined with cinchona alkaloids as chiral sources of carboxylate anion for the first time leading to a mixture of two regio-isomeric iodolactones with moderate enantioselectivity (exo- 18.5% ee, endo-35.0% ee) under mild reaction conditions. |
| 收录类别 | SCI |
| 语种 | 英语 |
| WOS记录号 | WOS:000220726500007 |
| 公开日期 | 2010-08-17 |
| 源URL | [http://202.98.16.49/handle/322003/15151]  |
| 专题 | 长春应用化学研究所_长春应用化学研究所知识产出_期刊论文 |
| 推荐引用方式 GB/T 7714 | Wang M,Gao LX,Yue W,et al. Reagent-controlled asymmetric iodolactonization using cinchona alkaloids as chiral sources[J]. synthetic communications,2004,34(6):1023-1032. |
| APA | Wang M,Gao LX,Yue W,&Mai WP.(2004).Reagent-controlled asymmetric iodolactonization using cinchona alkaloids as chiral sources.synthetic communications,34(6),1023-1032. |
| MLA | Wang M,et al."Reagent-controlled asymmetric iodolactonization using cinchona alkaloids as chiral sources".synthetic communications 34.6(2004):1023-1032. |
入库方式： OAI收割
来源：长春应用化学研究所
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