Ruthenium-Catalyzed, Keto-Directed, Site-Selective C-H Activation of Diverse Chromanones with Alkenes

被引:16
作者
Bakthadoss, Manickam [1 ]
Kumar, Polu Vijay [1 ]
Reddy, Tatiparthi Sushmitha [1 ]
机构
[1] Pondicherry Univ, Dept Chem, Pondicherry 605014, India
关键词
C-H activation; Directing groups; Site selectivity; Heterocycles; Fused-ring systems; ANTI-AIDS AGENTS; ARTOCARPUS-HETEROPHYLLUS; OXIDATIVE ALKENYLATION; EFFICIENT SYNTHESIS; BOND FORMATION; FLAVONOIDS; PALLADIUM; FUNCTIONALIZATION; ANTIOXIDANT; OLEFINATION;
D O I
10.1002/ejoc.201700513
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A simple and versatile approach towards the synthesis of highly functionalized C5-alkenylated chromanones in good yields in a regio- and stereoselective fashion was explored. This reaction takes place through chelation-aided oxidative coupling of keto-directed, site-selective C-H activation by using chromanones with alkenes in the presence of a ruthenium catalyst under mild conditions.
引用
收藏
页码:4439 / 4444
页数:6
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