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首页> 外文期刊>Organic letters >Asymmetric Construction of Spirocyclic Pyrrolidine-thia(oxa)zolidinediones via N,O-Ligand/Cu(I) Catalyzed 1,3-Dipolar Cycloaddition of Azomethine Ylides with 5-Alkylidene Thia(oxa)zolidine-2,4-diones
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Asymmetric Construction of Spirocyclic Pyrrolidine-thia(oxa)zolidinediones via N,O-Ligand/Cu(I) Catalyzed 1,3-Dipolar Cycloaddition of Azomethine Ylides with 5-Alkylidene Thia(oxa)zolidine-2,4-diones

机译:N,O-配体/ Cu(I)催化偶氮亚胺叶立德与1,5-亚炔基噻唑(oxa)zolidine-2,4-diones的1,3-偶极环加成反应,不对称构建螺环吡咯烷-噻唑(oxa)唑烷二酮

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摘要

A highly efficient asymmetric 1,3-dipolar cycloaddition of azomethine ylides to S-alkylidene thia(oxa)zolidine-2,4-diones catalyzed by a chiral N,O-ligand/Cu(CH3CN)(4)BF4 system is reported, affording structurally novel spirocyclic pyrrolidine-thia(oxa)zolidinediones with a spiro-heteroquaternary stereogenic center in good to excellent yields (up to 99%), with excellent levels of diastereo- and enantioselectivity (dr up to 99:1; ee up to 98%).
机译:据报道,通过手性N,O-配体/ Cu(CH3CN)(4)BF4体系催化的偶氮甲亚胺高效非对称的1,3-偶极环加成反应生成S-亚烷基硫杂氧杂唑烷-2,4-二酮。提供结构新颖的螺环吡咯烷-硫杂二恶唑烷二酮,具有螺-杂四元立体构型中心,产率高至优异(高达99%),非对映和对映选择性水平极佳(dr高达99:1; ee高达98 %)。

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