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Alkylation-Terminated Catellani Reactions by Cyclobutanol C–C Cleavage
Organic Letters ( IF 5.2 ) Pub Date : 2021-01-19 , DOI: 10.1021/acs.orglett.0c04018
Cui-Tian Wang 1 , Ming Li 1 , Ya-Nan Ding 1 , Wan-Xu Wei 1 , Zhe Zhang 1 , Xue-Ya Gou 1 , Rui-Qiang Jiao 1 , Ya-Ting Wen 1 , Yong-Min Liang 1
Affiliation  

This report describes the first application of a cyclobutanol ring-opening procedure in the Catellani termination reaction, which includes two β-carbon elimination processes. This tandem reaction features mild conditions, high yields, good functional group tolerance, and a broad substrate scope. Meanwhile, four types of electrophiles (N-benzoyloxyamines, alkyl iodides, aryl bromides, and benzyl chlorides) are quite compatible with this termination reaction for the construction of various types of polysubstituted aromatic hydrocarbons.

中文翻译:

环丁醇C–C裂解烷基化终止的Catellani反应

该报告描述了在Catellani终止反应中首次应用环丁醇开环程序,该程序包括两个β-碳消除过程。该串联反应具有温和的条件,高收率,良好的官能团耐受性和广泛的底物范围。同时,四种类型的亲电试剂(N-苯甲酰氧基胺,烷基碘,芳基溴化物和苄基氯)与这种终止反应完全相容,可用于构建各种类型的多取代芳烃。
更新日期:2021-02-05
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