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首页> 外文期刊>Journal of the American Chemical Society >Catalytic Asymmetric Synthesis of α-Amino Phosphonates Using Enantioselective Carbon-Carbon Bond-Forming Reactions
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Catalytic Asymmetric Synthesis of α-Amino Phosphonates Using Enantioselective Carbon-Carbon Bond-Forming Reactions

机译:对映选择性碳-碳键形成反应催化不对称合成α-氨基膦酸酯

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摘要

We have developed a highly enantioselelctive reaction of silicon enolates with N-acyl-α-iminophosphonates leading to nonracemic α-amino phosphonates. A copper (Ⅱ) complex was shown to be effective catalysts for this reaction, giving high yields and selectivities. It is noteworthy that this reaction opens a new pathway to various biologically important, nonracemic α-amino phosphonate derivatives. Studies into substrate variation, allowing access to libraries of α-amino phosphonates, and the application of this catalytic procedure to other reactions of N-acyl-α-iminophosphonates are currently underway in our laboratory.
机译:我们已经开发了烯醇硅与N-酰基-α-亚氨基膦酸酯的高度对映体化反应,从而产生非外消旋的α-氨基膦酸酯。铜(Ⅱ)配合物被证明是该反应的有效催化剂,具有高收率和选择性。值得注意的是,该反应为各种生物学上重要的,非外消旋的α-氨基膦酸酯衍生物开辟了一条新途径。目前正在实验室中研究底物变异,允许使用α-氨基膦酸酯的文库,并将该催化程序应用于N-酰基-α-亚氨基膦酸酯的其他反应。

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