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Org Biomol Chem ; 22(14): 2744-2748, 2024 Apr 03.
Artigo em Inglês | MEDLINE | ID: mdl-38470370

RESUMO

Phthalimides are prevalent in numerous pharmaceuticals, prompting various phthalimide syntheses through C-H activation. Nevertheless, the necessity for stoichiometric additives limits their practicality and versatility. Herein, we introduced diethyl dicarbonate as a carbonyl source for an additive-free carbonylation of benzamides. This transformation signifies an operationally simple and CO-free phthalimide synthesis.

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