| Literature DB >> 32663018 |
Jing Chen1,2, Yiwei Fu1, Yang Yu1, Jian-Rong Wang2, Yue-Wei Guo2, Hao Li1, Wei Wang1,3.
Abstract
An unprecedented organocatalytic enantioselective [4 + 2] cycloaddition reaction of vinyl quinolines with dienals is achieved with the synergistic activation of CH3SO3H and a chiral aminocatalyst. The power of the process is demonstrated by its high efficiency of the production of new synthetically and biologically valued chiral quinoline architectures in high yields and with excellent enantioselectivities.Entities:
Year: 2020 PMID： 32663018 DOI： 10.1021/acs.orglett.0c02137
Source DB: PubMed Journal: Org Lett ISSN： 1523-7052 Impact factor: 6.005