三氟甲基
试剂
化学
氟
光催化
组合化学
有机合成
过渡金属
绿色化学
可见光谱
有机化学
纳米技术
催化作用
反应机理
材料科学
烷基
光电子学
作者
Liang Jiang,Yisong Tang,Shuqi Li,Xing Peng,Rim Saffar Andaloussi,Xiao Yun Chen
标识
DOI:10.1002/asia.202401129
摘要
A novel protocol for the visible-light-driven synthesis of β-trifluoromethylated enamines has been developed, which operates without the use of transition metals or any photocatalysts, utilizing trifluoromethylthiosulfonium salts as the source of trifluoromethyl groups under mild conditions. According to this new protocol, more than 40 products have been prepared in moderate to good yields. In addition to eliminating the need for expensive or toxic transition metals and photocatalysts, this new methodology proves its potential scalability through air-stability, the use of safe and readily available reagents, a two-step one-pot procedure, and effective gram-scale reactions. This innovative approach not only demonstrates promise for green chemical synthesis but also offers a new pathway for the advancement of fluorine chemistry in sustainable organic synthesis.
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