作者: Masahito Murai , Koji Matsumoto , Yutaro Takeuchi , Kazuhiko Takai
DOI: 10.1021/ACS.ORGLETT.5B01373
关键词:
摘要: Use of a rhodium catalyst with electron-rich and bulky chiral diphosphine ligands having C2-symmetry allowed efficient dehydrogenative silylation the C(sp2)–H bond ferrocenes leading to benzosiloloferrocenes. The substrate scope was expanded hydrogermane hydrosilanes ruthenocene backbone, which resulted in new approach benzosilole- benzogermole-fused metallocenes.