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- W2044345120 abstract "Photooxygenation of azidoalkyl furans has revealed both a novel triazole formation method and a unique endoperoxide rearrangement. The key step of this method is a 3 + 2 cycloaddion of the azide to the endoperoxide intermediate. The reduction of the peroxide bond and two subsequent C–C bond cleavages provide a triazole having a newly formed carboxylic acid functionality. The reactions are clean and efficient with yields ranging from 60% to 90%." @default.
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- W2044345120 date "2014-01-23" @default.
- W2044345120 modified "2023-09-27" @default.
- W2044345120 title "ChemInform Abstract: Photooxygenation of Azidoalkyl Furans: Catalyst-Free Triazole and New Endoperoxide Rearrangement." @default.
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- W2044345120 doi "https://doi.org/10.1002/chin.201406161" @default.
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