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The catalytic resolution of racemic cyclic amines has been achieved by an enantioselective amidation reaction featuring an achiral N-heterocyclic carbene catalyst and a new chiral hydroxamic acid cocatalyst working in concert. The reactions proceed at room temperature, do not generate nonvolatile byproducts, and provide enantioenriched amines by aqueous extraction.
Because enzymes can increase reaction rates by enormous factors and tend to be very specific, Recommanded Product: 15862-72-3, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 15862-72-3
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Piperidine | C5H9011N – PubChem