Gifu Pharmaceutical University, 1-25-4 Daigaku-nishi, Gifu, 501-1196, Japan.
Org Lett. 2010 Apr 2;12(7):1620-3. doi: 10.1021/ol1003719.
Direct asymmetric aldol reactions of aldehydes with ketones in the presence of a catalytic amount of fluorous sulfonamide 4 and trifluoroacetic acid result in the corresponding aldol products in high yields with up to 96% ee. The fluorous organocatalyst 4 can be readily recovered from the reaction mixture by fluorous solid-phase extraction and could be reused without a significant loss of the catalytic activity and enantioselectivity.
在催化量的氟磺酰胺 4 和三氟乙酸的存在下,醛与酮的直接不对称羟醛反应得到相应的羟醛产物,产率高达 96%ee。氟相有机催化剂 4 可以通过氟固相萃取从反应混合物中轻易回收,并可以重复使用而不会显著损失催化活性和对映选择性。