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• W2014305989 abstract "Abstract Phenylazocarboxylic tert-butyl esters have recently been shown to be highly versatile building blocks due to their ability to undergo nucleophilic aromatic substitutions under mild conditions, particularly well with [18F]fluoride, and to act as precursors for aryl radicals. In this article, we now report first examples for cycloaddition reactions to phenylazocarboxylates. In a one-pot reaction with readily accessible glycine imines, a variety of highly substituted 1,2,4-triazoles could be obtained." @default.
• W2014305989 created "2016-06-24" @default.
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• W2014305989 date "2015-06-01" @default.
• W2014305989 modified "2023-10-12" @default.
• W2014305989 title "Cycloaddition reactions of glycine imine anions to phenylazocarboxylic esters – a new access to 1,3,5-trisubstituted 1,2,4-triazoles" @default.
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• W2014305989 doi "https://doi.org/10.1016/j.tet.2015.04.078" @default.
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