New explortion of 538-58-9

Because enzymes can increase reaction rates by enormous factors and tend to be very specific, Product Details of 538-58-9, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about Product Details of 538-58-9

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Stereoselective construction of highly functionalized azetidines via a [2 + 2]-cycloaddition

(Figure presented) A facile stereoselective synthesis of highly functionalized azetidines from a novel [2 + 2]-cycloaddition of 2-aminomalonates to chalcones is reported. The desired four-membered ring construction proceeded via a grind-promoted solvent-free Michael addition and a PhIO/Bu4NI mediated oxidative cyclization and afforded azetidines in moderate to good yields with excellent diastereoselectivities.

Because enzymes can increase reaction rates by enormous factors and tend to be very specific, Product Details of 538-58-9, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about Product Details of 538-58-9

Reference£º
Synthesis and Crystal Structure of a Chiral?C3-Symmetric Oxygen Tripodal Ligand and Its Applications to Asymmetric Catalysis,
Chiral lanthanide(III) complexes of sulphur¨Cnitrogen¨Coxygen ligand derived from aminothiourea and sodium?D-camphor-¦Â-sulfonate