Hexafluoroisobutylation of enolates through a tandem elimination/allylic shift/hydrofluorination reaction
Langue
EN
Article de revue
Ce document a été publié dans
Chemical Science. 2022-09-07, vol. 13, n° 33, p. 9507-9514
Résumé en anglais
The isobutyl side chain is a highly prevalent hydrophobic group in drugs, and it notably constitutes the side chain of leucine. Its replacement by a hexafluorinated version containing two CF groups may endow the target ...Lire la suite >
The isobutyl side chain is a highly prevalent hydrophobic group in drugs, and it notably constitutes the side chain of leucine. Its replacement by a hexafluorinated version containing two CF groups may endow the target compound with new and advantageous properties, yet this modification remains overlooked due to the absence of a general and practical synthetic methodology. Herein, we report the first general method to introduce the hexafluoroisobutyl group into ketoesters, malonates, 1,3-diketones, Schiff base esters and malononitrile. We demonstrated that the reaction occurs through an elimination/allylic shift/hydrofluorination cascade process which efficiently overcomes the usual fluoride β-elimination observed with α-CF-vinyl groups. We showed that with alkali metal bases, a pentafluorinated alkene is obtained predominantly, whereas the use of tetrabutylammonium fluoride (TBAF) allows hydrofluorination to occur. This tandem process represents a conceptually new pathway to synthesize bis-trifluoromethylated compounds. This methodology was applied to the multigram-scale synthesis of enantiopure ()-5,5,5,5',5',5'-hexafluoroleucine.< Réduire
Project ANR
Interactions supramoléculaires sélectives et directionnelles à base de synthons fluorés hautement polaires - ANR-20-CE06-0008
Unités de recherche