Sequential nucleophilic aromatic substitutions on cyanuric chloride: synthesis of BODIPY derivatives and mechanistic insights

Marques, Bruno da Silva; de Andrade, Karine Nascimento; Peixoto, Bárbara Pereira; dos Santos, Fernando Martins; Pedrosa, Leandro Ferreira; Fiorot, Rodolfo Goetze; Costa de Souza, Marcos

doi:10.1039/d4ob00683f

Org. Biomol. Chem.

2024

DOI: 10.1039/d4ob00683f

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Sequential nucleophilic aromatic substitutions on cyanuric chloride: synthesis of BODIPY derivatives and mechanistic insights

Bruno da Silva Marques,

Karine Nascimento de Andrade,

Bárbara Pereira Peixoto

et al.

Abstract: Concerning the nucleophilic aromatic substitution on cyanuric chloride the following preferential order for the substitution has been found: p-hydroxybenzaldehyde > 2-(pyridin-2-yl)ethanamine > aminoalkyl phosphoramidate.

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Sequential nucleophilic aromatic substitutions on cyanuric chloride: synthesis of BODIPY derivatives and mechanistic insights

Abstract: Concerning the nucleophilic aromatic substitution on cyanuric chloride the following preferential order for the substitution has been found: p-hydroxybenzaldehyde > 2-(pyridin-2-yl)ethanamine > aminoalkyl phosphoramidate.

Cited by 0 publications

References 58 publications

No citations

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