期刊
ORGANIC & BIOMOLECULAR CHEMISTRY
卷 17, 期 6, 页码 1531-1534出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c8ob02786b
关键词
-
资金
- National Natural Science Foundation of China [21302134]
An efficient and mild method was developed for the synthesis of 6-alkylated phenanthridines upon visible light irradiation. Bench-stable and easily handled redox-active Katritzky pyridinium salts derived from abundant amino acids/peptides were used as radical precursors for the alkylation of isocyanobiphenyl species. The reaction displays an excellent functional group tolerance and a potential utility for peptide functionalization, allowing access to desired products in good to excellent yields.
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