New types of biorelevantα-functional carboxylic acids and their application for peptide modification
E Windeisen1, R Pires, E Heistracher
1Organisch-Chemisches Institut, Technischen Universität München, Garching, Germany.
Amino Acids
|November 5, 2013
Abstract:
New methodology for the preparation of L-isoserine and its incorporation into N- and C-terminal position of peptides is described. Furthermore, the new protective group strategy allows regioselective functional group manipulation in multifunctional amino acids like serine and isoserine.
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