Department of Biomolecular Sciences, Section of Organic Chemistry and Organic Natural Compounds, University of Urbino "Carlo Bo" , Via I Maggetti 24, 61029 Urbino, Italy.
Department of Biomolecular Sciences, Section of Chemistry, University of Urbino "Carlo Bo" , Piazza Rinascimento 6, 61029 Urbino, Italy.
Org Lett. 2017 Feb 3;19(3):608-611. doi: 10.1021/acs.orglett.6b03775. Epub 2017 Jan 17.
A Pd(II)-catalyzed intramolecular oxidative C-H/C-H cross-coupling has been developed for the direct construction of valuable polycyclic heteroarene scaffolds. From a retrosynthetic point of view, the strategic formation of a C-C bond via C(sp)-H/C(sp)-H dehydrogenative coupling across C3,N-linked biheterocyclic precursors may be useful in de novo syntheses of indole-derived natural products and pharmaceuticals. The reaction exhibited good functional group/heterocycle tolerance, and a proposed mechanism involving an azoylpalladium complex is also supported.
Pd(II)催化的分子内氧化 C-H/C-H 交叉偶联反应已经被开发出来,用于直接构建有价值的多环杂芳烃骨架。从反合成的角度来看,通过 C(sp)-H/C(sp)-H 脱氢偶联在 C3,N 连接的双杂环前体之间形成 C-C 键可能有助于吲哚衍生的天然产物和药物的从头合成。该反应表现出良好的官能团/杂环耐受性,并且还支持涉及偶氮钯配合物的提出的反应机理。