Synthesis of pyrazoles by 1,3‐dipolar cycloaddition under aqueous micellar catalysis

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Ethyl diazoacetate (EDA), which is conveniently well prepared from ethyl glycinate and NaNO 2 , reacts in situ with alkynes in a drinking water micelle natural environment with out organic solvent to sort pyrazoles. The reaction is pH dependent, as in the presence of protic catalysis (H 2 SO 4  

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