二甲基甲酰胺
化学
氧化磷酸化
碳源
甲基化
有机化学
生物化学
基因
溶剂
作者
Kannika La‐ongthong,Teera Chantarojsiri,Darunee Soorukram,Pawaret Leowanawat,Vichai Reutrakul,Chutima Kuhakarn
标识
DOI:10.1002/asia.202400176
摘要
A benign electrochemical method to access 6-methylphenanthridines from 2-isocyanobiaryls using N,N-dimethylformamide (DMF) as a methyl source is reported. The protocol operates at ambient temperature without the need for harmful methylating reagents. Mechanistic studies suggested that DMF delivered a methylene synthon, followed by reduction at the cathode and tautomerization. The method offers environmental benefits by avoiding metal-based reagents and harsh conditions.
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