期刊
ORGANIC & BIOMOLECULAR CHEMISTRY
卷 10, 期 11, 页码 2209-2213出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c2ob06955e
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资金
- Grants-in-Aid for Scientific Research [22590007] Funding Source: KAKEN
A fluorous organocatalyst promotes direct asymmetric aldol reactions of aromatic aldehydes with ketones in brine to afford the corresponding anti-aldol products in high yield with up to 96% ee. Fluorous organocatalyst can be readily recovered by solid phase extraction using fluorous silica gel and reused without purification.
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