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New cleavable isocyanides for the combinatorial synthesis of α-amino acid analogue tetrazoles
Authors:Josef Mayer  Michael Umkehrer  Cédric Kalinski  Günther Ross  Christoph Burdack
Institution:a Priaton GmbH, Bahnhofstr. 9-15, D-82327 Tutzing, Germany
b Technical University Munich, Lichtenbergstr. 4, D-85747 Garching, Germany
Abstract:3-Substituted 3-isocyano propionates as new cleavable isocyanides in combinatorial tetrazole synthesis via Ugi-reaction are introduced. The obtained 5-substituted tetrazoles are transformed into carboxylic acid isosteric 5-substituted 1H-tetrazoles under basic cleavage conditions.
Keywords:Cleavable isocyanides  1H-Tetrazole  1H-Tetrazole U-4CR  Combinatorial chemistry
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