Regiodivergent Desymmetrization Reaction of meso-Azabicycloheptene Providing Two Enantioenriched Structural Isomers.
Yuxin ZhengYanze HuangPeng GaoHongyan LiuSuguru MurakamiRyosuke MatsubaraMasahiko HayashiPublished in: Organic letters (2021)
A novel catalytic asymmetric reaction is reported where the regiodivergent desymmetrisation of meso-azabicycloheptene via allylic oxidation using a single chiral copper catalyst produced two different, enantioenriched structural isomers in high optical purity starting from a single compound. The enantioselectivity of the two structurally isomeric compounds was enriched to >99.5% ee after derivatization.
Keyphrases
- ionic liquid
- electron transfer
- ms ms
- high resolution
- room temperature
- liquid chromatography tandem mass spectrometry
- visible light
- high performance liquid chromatography
- simultaneous determination
- gas chromatography mass spectrometry
- hydrogen peroxide
- high speed
- highly efficient
- metal organic framework
- solid phase extraction