| Literature DB >> 29791049 |
Yixuan Lin1,2, Kenward Vong1, Koji Matsuoka2, Katsunori Tanaka1,3,4.
Abstract
In previously reported work, AuIII complexes coordinated with 2-benzoylpyridine ligand, BPy-Au, were prebound to a protein and used to discover a novel protein-directed labeling approach with propargyl ester functional groups. In this work, further examination discovered that gold catalysts devoid of the 2-benzoylpyridine ligand (e.g., NaAuCl4) had significantly reduced levels of protein labeling. Mechanistic investigations then revealed that BPy-Au and propargyl esters undergo a rare example of C(sp2 )-C(sp) aryl-alkynyl cross-coupling, likely through spontaneous reductive elimination. Overall, these observations appear to suggest that BPy-Au-mediated, propargyl ester-based protein labeling acts via an activated ester intermediate, which contributes to our understanding of this process and will aid the expansion/optimization of gold-catalyst usage in future bioconjugation applications, especially in vivo.Entities:
Keywords: alkynes; amides; cross coupling; gold catalysis; protein conjugation
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Year: 2018 PMID: 29791049 DOI: 10.1002/chem.201802058
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236