Rh(Iii)-Catalyzed C6-Selective Acylmethylation And Carboxymethylation Of 2-Pyridones With Diazo Compounds

CHEMCATCHEM(2021)

Cited 6|Views2
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Abstract
Chelation-assisted C6-selective acylmethylation and carboxymethylation of 2-pyridones with diazo carbonyl compounds under [Cp*RhCl2](2)/AgSbF6 catalysis have been developed. Deesterificative C6-acylmethylation of 2-pyridones with diazo tert-butyl ester compounds proceeds effectively with the use of HOAc additive and hexafluoroisopropanol (HFIP) solvent, whereas switching to NaOAc additive and MeOH solvent enables efficient deacylative C6-carboxymethylation of 2-pyridones with alkyl 2-diazo-3-oxobutanoates. The procedures are characterized by excellent regioselectivity, high efficiency, broad substrate scope, wide functional group compatibility and gram-scalability. Preliminary mechanistic experiments are conducted to gain insights into the reaction mechanisms.
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Key words
2-pyridone, acylmethylation, carboxymethylation, rhodium, diazo compound
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