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• W2023542703 endingPage "12153" @default.
• W2023542703 startingPage "12144" @default.
• W2023542703 abstract "Brönsted acid-catalyzed one-pot synthesis of indoles from o-aminobenzyl alcohols and furans has been developed. This method operates via the in situ formation of aminobenzylfuran, followed by its recyclization into the indole core. The method proved to be efficient for substrates possessing different functional groups, including -OMe, -CO2Cy, and -Br. The resulting indoles can easily be transformed into diverse scaffolds, including 2,3- and 1,2-fused indoles, and indoles possessing an α,β-unsaturated ketone moiety at the C-2 position." @default.
• W2023542703 created "2016-06-24" @default.
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• W2023542703 date "2013-11-20" @default.
• W2023542703 modified "2023-09-27" @default.
• W2023542703 title "Brönsted Acid-Catalyzed One-Pot Synthesis of Indoles from <i>o</i>-Aminobenzyl Alcohols and Furans" @default.
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• W2023542703 doi "https://doi.org/10.1021/jo402132p" @default.
• W2023542703 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3923594" @default.
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• W2023542703 hasPublicationYear "2013" @default.
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