对映选择合成
硼酸
化学
胺气处理
催化作用
加合物
有机化学
产量(工程)
羧酸
材料科学
冶金
作者
Takahiro Horibe,Takashi Hazeyama,Yuto Nakata,Kazuki Takeda,Kazuaki Ishihara
标识
DOI:10.1002/anie.202007639
摘要
An enantioselective 1,4-addition of α,β-unsaturated carboxylic acids with cycloalkanones has been developed by using chiral amine-boronic acid cooperative catalysts. In the presence of a chiral amine and boronic acid, cycloalkanones and carboxylic acids are activated as chiral enamines and mixed anhydrides, respectively. The corresponding 1,4-adducts are obtained in high yield with high enantioselectivity. Furthermore, subsequent oxylactonization of the 1,4-adducts gives spirolactones with high diastereoselectivity.
科研通智能强力驱动
Strongly Powered by AbleSci AI