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Stereoselective Alkylation of Chiral Titanium(IV) Enolates with tert-Butyl Peresters

[Image: see text] Here, we present a new stereoselective alkylation of titanium(IV) enolates of chiral N-acyl oxazolidinones with tert-butyl peresters from Cα-branched aliphatic carboxylic acids, which proceeds through the decarboxylation of the peresters and the subsequent formation of alkyl radica...

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Detalles Bibliográficos
Autores principales: Pérez-Palau, Marina, Sanosa, Nil, Romea, Pedro, Urpí, Fèlix, López, Rosa, Gómez-Bengoa, Enrique, Font-Bardia, Mercè
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8609576/
https://www.ncbi.nlm.nih.gov/pubmed/34699246
http://dx.doi.org/10.1021/acs.orglett.1c03366
Descripción
Sumario:[Image: see text] Here, we present a new stereoselective alkylation of titanium(IV) enolates of chiral N-acyl oxazolidinones with tert-butyl peresters from Cα-branched aliphatic carboxylic acids, which proceeds through the decarboxylation of the peresters and the subsequent formation of alkyl radicals to produce the alkylated adducts with an excellent diastereoselectivity. Theoretical calculations account for the observed reactivity and the outstanding stereocontrol. Importantly, the resultant compounds can be easily converted into ligands for asymmetric and catalytic transformations.