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Efficient synthesis of isoindolones by intramolecular cyclisation of pyridinylbenzoic acids.

Atena B SoleaSining WangXiao-Song XueAurelien CrochetKatharina M FrommKendall N HoukOlimpia Mamula SteinerChristophe Allemann
Published in: Organic & biomolecular chemistry (2021)
A straightforward one-pot method for the synthesis of unreported pyrido-[2,1-a]isoindolones in excellent yield is described. Two novel isoindolones were synthesized and fully characterized. The alkyl substituents on the pyridine play an important role in the outcome of the reaction. The mechanism, investigated through DFT calculations, features an unprecendented intramolecular cyclization reaction involving a carboxylic acid activated by tosyl chloride and an electron-poor pyridinic nitrogen. This protocol completes the known strategies to obtain functionalized isoindolones.
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