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Diastereoselective Palladium-Catalyzed Conjugate Addition of Arylboronic Acids to α-Substituted Cyclic Enones
Synlett ( IF 1.7 ) Pub Date : 2017-08-23 , DOI: 10.1055/s-0036-1590742 Ang Gao 1 , Xiu-Yan Liu 1 , Chang-Hua Ding 1 , Xue-Long Hou 1, 2
Synlett ( IF 1.7 ) Pub Date : 2017-08-23 , DOI: 10.1055/s-0036-1590742 Ang Gao 1 , Xiu-Yan Liu 1 , Chang-Hua Ding 1 , Xue-Long Hou 1, 2
Affiliation
A palladium-catalyzed conjugate addition of arylboronic acids to α-substituted cyclic enones was developed to give α,β-disubstituted ketones with high diastereoselectivity. Mechanistic investigation showed that the high diastereoselectivity was realized through epimerization.
中文翻译:
非对映选择性钯催化的芳基硼酸与α-取代的环烯酮的共轭加成
开发了钯催化的芳基硼酸与 α-取代环烯酮的共轭加成,以得到具有高非对映选择性的 α,β-二取代酮。机理研究表明,高非对映选择性是通过差向异构化实现的。
更新日期:2017-08-23
中文翻译:
非对映选择性钯催化的芳基硼酸与α-取代的环烯酮的共轭加成
开发了钯催化的芳基硼酸与 α-取代环烯酮的共轭加成,以得到具有高非对映选择性的 α,β-二取代酮。机理研究表明,高非对映选择性是通过差向异构化实现的。