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Direct synthesis of sensitive selenocysteine peptides by the Ugi reaction
Muhammad Abbas1, Ludger A Wessjohann
1Leibniz-Institut für Pflanzenbiochemie, Weinberg 3, D-06120 Halle (Saale), Germany.
Organic & Biomolecular Chemistry
|November 2, 2012
Abstract:
Ammonia and selenoaldehydes are both problematic components in Ugi reactions. Here we report the efficient direct multicomponent synthesis of sensitive selenocysteine peptides without the use of convertible (protected) primary amines, including suitable deprotection protocols for selenols.

