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中文摘要：
Binaphthyl sulfonimides 被开发了催化酉同类的不对称的迈克尔增加到 alkylidene malonates ，负担得起相应迈克尔产品在对高收益(多达98%)与好对优秀 diastereoselectivity 好(依赖 99:1 医生)并且在把环境地良性的水用作溶剂的温和条件下面的 enantioselectivity (多达92% ee )。
英文摘要：
Binaphthyl sulfonimides have been developed to catalyze the asymmetric Michael addition of ketone to alky- lidene malonates, affording the corresponding Michael products in good to high yields （up to 98%） with good to excellent diastereoselectivity （up to 99 ; 1 dr） and enantioselectivity （up to 92% ee） under mild conditions using environmentally benign water as the solvent.
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