摘要
Chiral β-amino alcohols and vicinal diamine structures are undoubtedly important and ubiquitous backbones in pharmaceutical drugs and natural products.Herein,an iridium-catalyzed asymmetric cascade ring-opening/allylic amination reaction was developed between vinyl heterocyclic propanes and aromatic or aliphatic amine derivatives,which delivered optically activeβ-amino alcohols and vicinal diamines in good yields with excellent enantioselectivities.The reported transformations were provided with broad amino substrate scope and substituent tolerance,and the synthetic utility was also demonstrated by robust and downstream transformations.The current protocol established a practical synthetic platform for diverse optically active four carbon aliphatic amino alcohols and vicinal diamines.
基金
support of the National Natural Science Foundation of China(22171199)
the program for New Century Excellent Talents in University(NCET-12-0743)
a project funded by the Priority Academic Program Development of Jiangsu Higher Education Institutions(PAPD).
