期刊
ORGANIC LETTERS
卷 11, 期 20, 页码 4648-4651出版社
AMER CHEMICAL SOC
DOI: 10.1021/ol901920s
关键词
-
资金
- CNRS
- ICSN
The beta-ICD (1a) or beta-ICD-amide(1e)-catalyzed aza-Morita-Baylis-Hillman reaction between N-sulfonylimines 3 and alkyl vinyl ketones 4 produced the (R)-enriched adducts 5. By adding a catalytic amount beta-naphthol (2a), the enantioselectivity of the same reaction was inversed leading to (S)-5 in excellent yields and enantioselectivities. Both aromatic and aliphatic imines are accepted as substrates for this reaction.
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。
推荐
暂无数据