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• W2015146016 endingPage "177" @default.
• W2015146016 startingPage "170" @default.
• W2015146016 abstract "Mild conditions have been developed to achieve Pd-catalyzed homocoupling of indoles with excellent regioselectivity in the presence of Cu(OAc)2·H2O in DMSO at room temperature in high efficiency. This method provides a simple route to 2,3′-biindolyls from the electron-rich to moderately electron-poor indoles. The reaction tolerates the bromide substituent on indoles. In addition, a one-pot approach to C3-position acetoxylated biindolyls is realized via palladium catalysis by the use of AgOAc under oxygen atmosphere as oxidants." @default.
• W2015146016 created "2016-06-24" @default.
• W2015146016 creator A5019111779 @default.
• W2015146016 creator A5034984218 @default.
• W2015146016 creator A5088486032 @default.
• W2015146016 date "2009-12-03" @default.
• W2015146016 modified "2023-10-17" @default.
• W2015146016 title "Palladium-Catalyzed Regioselective Oxidative Coupling of Indoles and One-Pot Synthesis of Acetoxylated Biindolyls" @default.
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• W2015146016 doi "https://doi.org/10.1021/jo902265s" @default.
• W2015146016 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/19957925" @default.
• W2015146016 hasPublicationYear "2009" @default.
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