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Pd-catalyzed C–H arylation of benzothioamides with boronic acids using thioamides as directing groups
Organic Chemistry Frontiers ( IF 5.4 ) Pub Date : 2017-08-04 00:00:00 , DOI: 10.1039/c7qo00532f Kai-Xiang Tang 1, 2, 3, 4, 5 , Chun-Meng Wang 1, 2, 3, 4, 5 , Tian-Hong Gao 1, 2, 3, 4, 5 , Cong Pan 1, 2, 3, 4, 5 , Li-Ping Sun 1, 2, 3, 4, 5
Organic Chemistry Frontiers ( IF 5.4 ) Pub Date : 2017-08-04 00:00:00 , DOI: 10.1039/c7qo00532f Kai-Xiang Tang 1, 2, 3, 4, 5 , Chun-Meng Wang 1, 2, 3, 4, 5 , Tian-Hong Gao 1, 2, 3, 4, 5 , Cong Pan 1, 2, 3, 4, 5 , Li-Ping Sun 1, 2, 3, 4, 5
Affiliation
The Pd(II)-catalyzed C–H arylation of benzothioamides with boronic acids using thioamides as directing groups, prevalent organic motifs found in vital biological and pharmaceutical molecules, has been achieved for the first time. The reactions proceed with high functional group tolerance in yields of 21–84%.
中文翻译:
以硫代酰胺为导向基团,Pd催化苯并硫代酰胺与硼酸的CH芳基化
首次实现了以硫代酰胺为导向基团的苯并硫代酰胺与硼酸的Pd(II)催化的CHH芳基化反应,这是重要的生物和药物分子中常见的有机基序。反应以较高的官能团耐受性进行,产率为21–84%。
更新日期:2017-10-25
中文翻译:
以硫代酰胺为导向基团,Pd催化苯并硫代酰胺与硼酸的CH芳基化
首次实现了以硫代酰胺为导向基团的苯并硫代酰胺与硼酸的Pd(II)催化的CHH芳基化反应,这是重要的生物和药物分子中常见的有机基序。反应以较高的官能团耐受性进行,产率为21–84%。