化学
三苯基膦
芳基
级联
三苯基氧化膦
碳酸盐
氧化物
有机化学
组合化学
药物化学
催化作用
烷基
色谱法
作者
Wenhao Wang,Daming Feng,Ping Zhang,Peng Huang,Chunhua Ge
标识
DOI:10.1021/acs.joc.4c00804
摘要
A novel method for synthesizing substituted 4-chloroquinolines has been devised, utilizing a cascade reaction of N-aryl enaminones promoted by bis(trichloromethyl) carbonate (BTC) and triphenylphosphine oxide (TPPO). This approach features accessible starting materials, a broad substrate range, extensive functional group compatibility, gentle reaction conditions, and straightforward operation. Its versatility is evidenced by its facile scalability and suitability for late-stage derivatization. A plausible mechanism involving α-carbonylation, 6π-azaelectrocyclization, and dehydroxychlorination sequence is proposed.
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