期刊论文详细信息
| Molecules | |
| Enantioselective Evans-Tishchenko Reduction of b-Hydroxyketone Catalyzed by Lithium Binaphtholate | |
| Tomonori Ichibakase1  Masato Nakatsu1  | |
| [1] Graduate School of Pharmaceutical Sciences, Kumamoto University, 5-1 Oe-honmachi, Kumamoto 862-0973, Japan | |
| 关键词: Evans-Tishchenko reduction; lithium binaphtholate; b-hydroxyketone; 1; 3-diol; enantioselectivity; | |
| DOI : 10.3390/molecules16065008 | |
| 来源: mdpi | |
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【 摘 要 】
Lithium diphenylbinaphtholate catalyzed the enantioselective Evans-Tishchenko reduction of achiral b-hydroxyketones to afford monoacyl-protected 1,3-diols with high stereoselectivities. In the reaction of racemic b-hydroxyketones, kinetic optical resolution occurred in a highly stereoselective manner.
【 授权许可】
CC BY
This is an open access article distributed under the Creative Commons Attribution License (CC BY) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
【 预 览 】
| Files | Size | Format | View |
|---|---|---|---|
| RO202003190049254ZK.pdf | 211KB |
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