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- W2914365800 abstract "Furstner and Mamane described a synthesis of benzo[g] indoles using PtCl2, and Furstner and Davies subsequently generalized this indolization. The atmosphere of carbon monoxide accelerates the reaction. Yu and colleagues extended the Pt-catalyzed cyclization of o-alkynylanilines in the presence of ethyl propiolate and dimethyl acetylenedicarboxylate to give 2,3-disubstituted indoles. Nakamura's group described a novel Pt-catalyzed dehydroalkoxylation/cyclization cascade process to afford a unique synthesis of the indoloisoquinolinone and indoloquinazolinone ring systems. This research group also reported a similar Pt-catalyzed synthesis of indole-3-carbamides and indole-3-carboxy-lates from o-alkynylphenylureas and o-alkynylphenyl carbamates, respectively. The Pt-catalyzed C-H functionalization of 2-aminobiphenyls, in water as the reoxidant, gave carbazoles as discovered by Matsubara and Yamamoto." @default.
- W2914365800 created "2019-02-21" @default.
- W2914365800 creator A5049245360 @default.
- W2914365800 date "2016-06-17" @default.
- W2914365800 modified "2023-09-23" @default.
- W2914365800 title "Platinum-Catalyzed Indole Ring Synthesis" @default.
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- W2914365800 doi "https://doi.org/10.1002/9781118695692.ch83" @default.
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