Fehler S, Pratsch G, Östreicher C, Fürst M, Pischetsrieder M, Heinrich M (2016)
Publication Status: Published
Publication Type: Journal article, Original article
Publication year: 2016
Publisher: Elsevier Ltd
Book Volume: 72
Pages Range: 7888-7893
Journal Issue: 48
DOI: 10.1016/j.tet.2016.04.084
The radical arylation of the phenolic side chain of tyrosine in peptides was investigated. Aryl radicals were generated from aryldiazonium salts using titanium(III) chloride as stoichiometric reductant. Due to the high selectivity with which 3-aryltyrosine derivatives were formed, this reaction type represents a new strategy for the direct functionalization of peptides.
APA:
Fehler, S., Pratsch, G., Östreicher, C., Fürst, M., Pischetsrieder, M., & Heinrich, M. (2016). Radical arylation of tyrosine residues in peptides. Tetrahedron, 72(48), 7888-7893. https://doi.org/10.1016/j.tet.2016.04.084
MLA:
Fehler, Stefanie, et al. "Radical arylation of tyrosine residues in peptides." Tetrahedron 72.48 (2016): 7888-7893.
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