Department of Frontier Materials, Nagoya Institute of Technology, Gokiso, Nagoya, 466-8555, Japan.
Org Lett. 2011 Aug 5;13(15):3972-5. doi: 10.1021/ol201490e. Epub 2011 Jun 24.
The organocatalyzed regioselective allylic trifluoromethylation of Morita-Baylis-Hillman adducts using Ruppert-Prakash reagent was achieved in high to excellent yields via a successive S(N)2'/S(N)2' mode for the first time. The reaction was extended to the asymmetric allylic trifluoromethylation by the use of a bis-cinchona alkaloid catalyst with high enantioselectivities up to 94% ee.
首次通过连续的 S(N)2'/S(N)2' 模式,使用 Ruppert-Prakash 试剂实现了 Morita-Baylis-Hillman 加成物的高至优异产率的有机催化区域选择性烯丙基三氟甲基化。通过使用双金鸡纳碱催化剂,该反应得到了扩展,对映选择性高达 94%ee。