4.6 Article

Highly efficient asymmetric aldol reaction in brine using a fluorous sulfonamide organocatalyst

期刊

ORGANIC & BIOMOLECULAR CHEMISTRY
卷 10, 期 11, 页码 2209-2213

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c2ob06955e

关键词

-

资金

  1. Grants-in-Aid for Scientific Research [22590007] Funding Source: KAKEN

向作者/读者索取更多资源

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.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据