N-aryl pyrazoles: DFT calculations of CH acidity and deprotonative metallation using a combination of lithium and zinc amides. - Archive ouverte HAL
Article Dans Une Revue Organic & Biomolecular Chemistry Année : 2011

N-aryl pyrazoles: DFT calculations of CH acidity and deprotonative metallation using a combination of lithium and zinc amides.

Résumé

A series of N-aryl and N-heteroaryl pyrazoles have been deproto-metallated using a 2,2,6,6-tetramethylpiperidino-based mixed lithium-zinc combination. Mono-, di-, and tri-iodides have been obtained after subsequent trapping with iodine, depending on the substrate and on the quantity of base used. The results have been discussed in the light of the CH acidities of the substrates, determined both in the gas phase and in THF solution using the DFT B3LYP method.

Domaines

Chimie organique
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Dates et versions

hal-00737022 , version 1 (01-08-2014)

Identifiants

Citer

Floris Chevallier, Yury S. Halauko, Christelle Pecceu, Ibrahim F. Nassar, To Uyen Dam, et al.. N-aryl pyrazoles: DFT calculations of CH acidity and deprotonative metallation using a combination of lithium and zinc amides.. Organic & Biomolecular Chemistry, 2011, 9 (12), pp.4671-4684. ⟨10.1039/c1ob05267e⟩. ⟨hal-00737022⟩
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