Publications by authors named "Cheng-Li He"

Article Synopsis
  • Researchers are focusing on enhancing enzymatic methods for creating valuable molecules in synthetic chemistry and pharmaceuticals, particularly chiral thiiranes, due to limited existing synthesis methods.
  • A new biocatalytic thionation approach has been developed, which uses a specially engineered halohydrin dehalogenase (HHDH) to selectively open epoxide rings with thiocyanate and transform them into thiiranes.
  • The engineered HHDH enabled successful production of various thiiranes with significant yield and enantioselectivity, showcasing the method's efficiency through large-scale synthesis and further useful transformations.
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We report the discovery of an unusual halohydrin dehalogenase, HHDHamb, that can work under relatively low acidic conditions and extremely low temperatures for the bio-nitration of epoxides using nitrite as a nitrating agent. The bio-nitration strategy exhibits high chemo-, regio-, and enantioselectivity, catalyzing the kinetic resolution of various epoxides to enantiopure β-nitroalcohols with nitro-bearing stereocenters in up to 41 % isolated yield and >99 % enantiomeric excess (ee). Additionally, the bio-nitration method displays a high reaction efficiency and can be performed on a gram scale.

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The main targets of this work were to evaluate the antioxidative properties of flavonoids in Jerusalem artichoke ( L.) leaves and quantitatively determine their contents. 2,2-diphenyl-1-picrylhydrazyl (DPPH), 2,2-azino-bis (3-ethylbenzothiazoline)-6-sulphonic acid (ABTS) and hydroxyl free radicals scavenging assays were performed to determine their antioxidative capacities.

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