Photoinduced decarboxylative azidation of cyclic amino acids?
Organic & Biomolecular Chemistry Pub Date: 2018-12-26 DOI: 10.1039/C8OB02702A
Abstract
The direct decarboxylative azidation of cyclic α-amino acids has been achieved via visible light-mediated organo-photoredox catalysis. This synthetic strategy allows the simple preparation of azide-contaning building blocks and has been used in the selective modification of N-terminal proline residues of two di-peptides.
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Journal Name：Organic & Biomolecular Chemistry
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CAS no.: 89640-58-4
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