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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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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
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author Pérez-Palau, Marina
Sanosa, Nil
Romea, Pedro
Urpí, Fèlix
López, Rosa
Gómez-Bengoa, Enrique
Font-Bardia, Mercè
author_facet Pérez-Palau, Marina
Sanosa, Nil
Romea, Pedro
Urpí, Fèlix
López, Rosa
Gómez-Bengoa, Enrique
Font-Bardia, Mercè
author_sort Pérez-Palau, Marina
collection PubMed
description [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.
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spelling pubmed-86095762021-11-24 Stereoselective Alkylation of Chiral Titanium(IV) Enolates with tert-Butyl Peresters Pérez-Palau, Marina Sanosa, Nil Romea, Pedro Urpí, Fèlix López, Rosa Gómez-Bengoa, Enrique Font-Bardia, Mercè Org Lett [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. American Chemical Society 2021-10-26 2021-11-19 /pmc/articles/PMC8609576/ /pubmed/34699246 http://dx.doi.org/10.1021/acs.orglett.1c03366 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Pérez-Palau, Marina
Sanosa, Nil
Romea, Pedro
Urpí, Fèlix
López, Rosa
Gómez-Bengoa, Enrique
Font-Bardia, Mercè
Stereoselective Alkylation of Chiral Titanium(IV) Enolates with tert-Butyl Peresters
title Stereoselective Alkylation of Chiral Titanium(IV) Enolates with tert-Butyl Peresters
title_full Stereoselective Alkylation of Chiral Titanium(IV) Enolates with tert-Butyl Peresters
title_fullStr Stereoselective Alkylation of Chiral Titanium(IV) Enolates with tert-Butyl Peresters
title_full_unstemmed Stereoselective Alkylation of Chiral Titanium(IV) Enolates with tert-Butyl Peresters
title_short Stereoselective Alkylation of Chiral Titanium(IV) Enolates with tert-Butyl Peresters
title_sort stereoselective alkylation of chiral titanium(iv) enolates with tert-butyl peresters
url 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
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