Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/183605
Title: Stereoselective Alkylation of Chiral Titanium(IV) Enolates with tert-Butyl Peresters
Author: Pérez-Palau, Marina
Sanosa, Nil
Romea, Pedro
Urpí Tubella, Fèlix
López, Rosa
Gómez-Bengoa, Enrique
Font Bardia, Ma. Mercedes
Keywords: Alcohols
Anions
Estereoquímica
Alcohols
Anions
Stereochemistry
Issue Date: 19-Nov-2021
Publisher: American Chemical Society
Abstract: 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.
Note: Reproducció del document publicat a: https://doi.org/10.1021/acs.orglett.1c03366
It is part of: Organic Letters, 2021, vol. 23, num. 22, p. 8852-8856
URI: http://hdl.handle.net/2445/183605
Related resource: https://doi.org/10.1021/acs.orglett.1c03366
ISSN: 1523-7060
Appears in Collections:Articles publicats en revistes (Química Inorgànica i Orgànica)

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