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- W3108032558 abstract "The synthesis of variously substituted indolo[2,3-c]quinolin-6(7H)-ones was developed via Pd-catalyzed intramolecular C-H arylation. This method highlights a strategy for preparing indoloquinoline precursors bearing versatile functional groups and provides a new approach for the synthesis of antimalarial isoneocryptolepine analogues. The plausible ring closure mechanism was examined with quantum chemical calculations, where a trigonal bipyramidal concerted metalation-deprotonation transition state is presumable." @default.
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- W3108032558 date "2020-11-30" @default.
- W3108032558 modified "2023-09-27" @default.
- W3108032558 title "Synthesis of Indolo[2,3-<i>c</i>]quinolin-6(7<i>H</i>)-ones and Antimalarial Isoneocryptolepine. Computational Study on the Pd-Catalyzed Intramolecular C–H Arylation" @default.
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- W3108032558 doi "https://doi.org/10.1021/acs.joc.0c01832" @default.
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