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Double C–H Functionalization of Indoles via Three-Component Reactions/CuCl2‑Catalyzed Aerobic Dehydrogenative Coupling for the Synthesis of Polyfunctional Cyclopenta[b]indoles

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Figshare2016-08-29 更新2026-04-29 收录
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https://figshare.com/articles/dataset/Double_C_H_Functionalization_of_Indoles_via_Three-Component_Reactions_CuCl_sub_2_sub_Catalyzed_Aerobic_Dehydrogenative_Coupling_for_the_Synthesis_of_Polyfunctional_Cyclopenta_i_b_i_indoles/3581592
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A sequential Rh2(OAc)4-catalyzed multicomponent reaction and CuCl2-catalyzed postcyclization process is developed to build polyfunctional cyclopenta­[b]­indoles in good yields with high diastereoselectivities in an atom- and step-economic fashion. The key discovery in this process is the CuCl2-catalyzed intramolecular aerobic dehydrogenative Csp2–Csp2 cross-coupling of indole C2 with an enol functionality. Mechanistic studies including X-ray photoelectron spectroscopy analysis suggest that the catalytic cycle involves Cu­(II) and Cu­(I). This coupling reaction represents a unique example of aerobic Cu-catalyzed direct coupling of indoles with enols under mild conditions.
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2016-08-29
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