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- W2022387412 endingPage "6932" @default.
- W2022387412 startingPage "6923" @default.
- W2022387412 abstract "A variety of 3-vinyl-substituted imidazo[1,5-a]indole derivatives were synthesized by intramolecular Pd-catalyzed cyclization of the title allenamides through either a domino carbopalladation/exo-cyclization process or a novel hydroamination reaction that proceeds smoothly under microwave irradiation. Both the observed pathways involve a π-allyl-palladium(II) complex arising from insertion of the allene group into a palladium(II) species, the latter being formed in situ by the intervention of an aryl iodide or of the N-H group. In both cases, the role of nucleophile is covered by the indole nitrogen." @default.
- W2022387412 created "2016-06-24" @default.
- W2022387412 creator A5008699651 @default.
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- W2022387412 creator A5024834000 @default.
- W2022387412 creator A5050534821 @default.
- W2022387412 creator A5055624429 @default.
- W2022387412 creator A5062563965 @default.
- W2022387412 date "2010-09-23" @default.
- W2022387412 modified "2023-10-18" @default.
- W2022387412 title "Tunable Pd-Catalyzed Cyclization of Indole-2-carboxylic Acid Allenamides: Carboamination vs Microwave-Assisted Hydroamination" @default.
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