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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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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. |
format | Online Article Text |
id | pubmed-8609576 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
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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