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Ytterbium(III) Trifluoromethanesulfonate Catalyzed Ring‐Opening C(sp3)−N Bond Formation of Benzoxazoles with Propargylic Alcohols
ChemCatChem ( IF 3.8 ) Pub Date : 2016-08-17 , DOI: 10.1002/cctc.201600606 Wenfei Liu 1 , Yongqing Sun 1 , Haiying Zhao 1 , Baoguo Li 1 , Shufeng Chen 1
ChemCatChem ( IF 3.8 ) Pub Date : 2016-08-17 , DOI: 10.1002/cctc.201600606 Wenfei Liu 1 , Yongqing Sun 1 , Haiying Zhao 1 , Baoguo Li 1 , Shufeng Chen 1
Affiliation
A novel ytterbium(III) trifluoromethanesulfonate [Yb(OTf)3]‐catalyzed ring‐opening C(sp3)−N bond formation reaction of benzoxazole with propargylic alcohols was established. This reaction uses readily available starting materials and is operationally simple; it thus represents a practical method for the construction of highly functionalized substituted benzenes bearing aldehyde, propargylamine, and hydroxy groups with high atom economy.
中文翻译:
三氟甲磺酸(III)催化苯并恶唑与丙醇的开环C(sp3)-N键形成
建立了新型的三氟甲烷磺酸y(III)[Yb(OTf)3 ]催化的苯并恶唑与炔丙醇的开环C(sp 3)-N键形成反应。该反应使用容易获得的起始原料,并且操作简单。因此,它代表了一种实用的方法,用于以高原子经济性构建带有醛,炔丙基胺和羟基的高官能度取代苯。
更新日期:2016-08-17
中文翻译:
三氟甲磺酸(III)催化苯并恶唑与丙醇的开环C(sp3)-N键形成
建立了新型的三氟甲烷磺酸y(III)[Yb(OTf)3 ]催化的苯并恶唑与炔丙醇的开环C(sp 3)-N键形成反应。该反应使用容易获得的起始原料,并且操作简单。因此,它代表了一种实用的方法,用于以高原子经济性构建带有醛,炔丙基胺和羟基的高官能度取代苯。