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- W4362473011 endingPage "108398" @default.
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- W4362473011 abstract "A new palladium-catalyzed annulative allylic alkylation (AAA) reaction of 2-(indol-2-yl)phenols with dual allylic electrophiles such as isobutylene dicarbonate and butene dicarbonate is described, leading to the regioselective synthesis of tetracyclic medium-sized cyclic ethers possessing a bridged aryl-indole scaffold, namely, benzo[2,3]oxocino[4,5-b]indoles and benzo[2,3]oxepino[4,5-b]indoles, in good to excellent yields. This protocol demonstrates a broad substrate scope, good compatibility with substituents and high regioselectivity, providing a catalytic and flexible method for creating bridged aryl-indole skeletons." @default.
- W4362473011 created "2023-04-05" @default.
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- W4362473011 date "2023-12-01" @default.
- W4362473011 modified "2023-10-16" @default.
- W4362473011 title "Palladium-catalyzed annulative allylic alkylation for regioselective construction of indole-fused medium-sized cyclic ethers" @default.
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- W4362473011 doi "https://doi.org/10.1016/j.cclet.2023.108398" @default.
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