Lithium acetate-catalyzed Michael reaction between trimethylsilyl enolates and alpha,beta-unsaturated carbonyl compounds in DMF proceeded smoothly to afford the corresponding Michael-adducts in good to high yields. Hindered alpha, beta-unsaturated ketones also behaved as an excellent Michael-acceptor in the above reaction at room temperature.
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