首页> 外文期刊>Advanced synthesis & catalysis >Gold(I)-Catalyzed Regio- and Stereoselective 1,3-Dipolar Cycloaddition Reactions of l-(l-Alkynyl)cyclopropyl Oximes with Nitrones: A Modular Entry to Highly Substituted Pyrrolo[3,4-d] [l,2]oxazepines
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Gold(I)-Catalyzed Regio- and Stereoselective 1,3-Dipolar Cycloaddition Reactions of l-(l-Alkynyl)cyclopropyl Oximes with Nitrones: A Modular Entry to Highly Substituted Pyrrolo[3,4-d] [l,2]oxazepines

机译:金(I)催化的1-(1-炔基)环丙基肟与硝基的区域和立体选择性1,3-偶极环加成反应:高度取代的吡咯并[3,4-d] [l,2]氮杂ze庚因的模块入口

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摘要

An efficient approach for the synthesis of highly substituted pyrrolo[3,4-d][l,2]oxazepines has been achieved by gold(I)-catalyzed 1,3-dipolar cycloaddition reactions of l-(l-alkynyl)cyclopropyl oximes with nitrones in good to excellent yields as a single diastereomer. A complete chirality transfer was observed in this transformation.
机译:通过金(I)催化的1-(1-炔基)环丙基肟的1,3-偶极环加成反应,已经获得了一种高效合成高度取代的吡咯并[3,4-d] [l,2]氮杂ze庚烷的方法。含有硝酮的单一非对映异构体,收率好至极佳。在该转化中观察到完全手性转移。

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