Simple quinine as an organocatalyst mediates the addition of various naphthols to halogenated quinones to afford non‐C2‐symmetrical, axially chiral biaryl products, which are promising compounds as chiral ligands and organocatalysts. The rotational barrier required to have two distinct atropisomers has been evaluated in the products generated from the addition of naphthols to various quinones by means
                                    简单的
奎宁作为有机催化剂可介导将各种
萘酚添加到卤代醌中,以提供非C 2对称的轴向手性联芳基产品,这些化合物有望用作手性
配体和有机催化剂。已通过DFT计算和HPLC在将
萘酚添加到各种醌中生成的产物中评估了具有两种不同的阻转异构体所需的旋转势垒。必须使用卤代醌作为试剂,以得到结构稳定的对映体产物,该产物可以良好的收率和立体选择性获得。这些化合物也已以克量制备,并重结晶至接近对映体纯度。