Photomodulation of the Conformation of Cyclic Peptides with Azobenzene Moieties in the Peptide Backbone

Abstract
The cistrans photoisomerization of the azobenzene building block 4‐(4‐aminophenylazo)benzoic acid incorporated in a cyclic peptide (see scheme) facilitated a two‐state transition of the peptide chain from a rigid constrained conformation in the trans isomer into the largely free conformational space of the cis isomer.

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