Highly Enantioselective Synthesis of [1,2,4]Triazino[5,4- a ]isoquinoline Derivatives via (3 + 3) Cycloaddition Reactions of Diazo Compounds and Isoquinolinium Methylides.
Wei WuXiao YanXiaofeng LiYanqiang NingLei HuLei ZhuQin OuyangYungui PengPublished in: Organic letters (2022)
An array of chiral [1,2,4]triazino[5,4- a ]isoquinoline derivatives were obtained in excellent yields (up to 98%) and with excellent enantioselectivities (up to 99% ee) via a new highly asymmetric (3 + 3) cycloaddition reaction of diazo compounds and isoquinolinium methylides, with a bifunctional chiral phase-transfer catalyst (PTC). Density functional theory calculations show that PTC has a bridge role in the deprotonation/protonation process. The obtained products were transformed into densely functionalized polycyclic heterocompounds with multiple stereocenters.
Keyphrases
- density functional theory
- ionic liquid
- molecular dynamics
- capillary electrophoresis
- highly efficient
- metal organic framework
- structure activity relationship
- high resolution
- room temperature
- quantum dots
- carbon dioxide
- mass spectrometry
- gold nanoparticles
- molecularly imprinted
- visible light
- solid state
- molecular dynamics simulations