N-alpha-t-Butyloxycarbonyl-4-Ethynyl-L-phenylalanine

N-alpha-t-Butyloxycarbonyl-4-Ethynyl-L-phenylalanine


This Boc-protected non canonical substituted phenylalanine contains a chemical handle, e.g. for post-translational biorthogonal conjugation reactions, e.g. by copper(I)-catalyzed azide-alkyne cycloadditions (CuAAC), an efficient Click Chemistry Reaction. CuAAC is orthogonal in the context of proteins and other cellular components, enabling applications in bacteria and mammalian cell lines. Furthermore, alkyne-alkyne coupling reactions are evaluated in peptide chemistry to cyclize or functionalize peptidic backbones.

Molecular structure of the compound BP-46777
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