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New anionic cobalt(III) complexes enable enantioselective synthesis of spiro-fused oxazoline and iodoacetal derivatives

Anionic salicylimine-based cobalt (III) complexes featuring chiral ligands derived from isoleucine amino acids were used as efficient bifunctional phase-transfer catalysts for electrophilic iodination of enol ethers. The Brønsted acids of these complexes enabled the enantioselective asymmetric iodoc...

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Autores principales: Salem, Mohamed S. H., Takizawa, Shinobu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9606352/
https://www.ncbi.nlm.nih.gov/pubmed/36311431
http://dx.doi.org/10.3389/fchem.2022.1034291
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author Salem, Mohamed S. H.
Takizawa, Shinobu
author_facet Salem, Mohamed S. H.
Takizawa, Shinobu
author_sort Salem, Mohamed S. H.
collection PubMed
description Anionic salicylimine-based cobalt (III) complexes featuring chiral ligands derived from isoleucine amino acids were used as efficient bifunctional phase-transfer catalysts for electrophilic iodination of enol ethers. The Brønsted acids of these complexes enabled the enantioselective asymmetric iodocyclization of enol ethers, furnishing spiro-fused oxazoline derivatives in high yields with up to 90:10 er. In addition, chiral cobalt (III) complexes catalyze the asymmetric intermolecular iodoacetalization of enol ethers with various alcohols to afford 3-iodoacetal derivatives in high yields with up to 92:8 er.
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spelling pubmed-96063522022-10-28 New anionic cobalt(III) complexes enable enantioselective synthesis of spiro-fused oxazoline and iodoacetal derivatives Salem, Mohamed S. H. Takizawa, Shinobu Front Chem Chemistry Anionic salicylimine-based cobalt (III) complexes featuring chiral ligands derived from isoleucine amino acids were used as efficient bifunctional phase-transfer catalysts for electrophilic iodination of enol ethers. The Brønsted acids of these complexes enabled the enantioselective asymmetric iodocyclization of enol ethers, furnishing spiro-fused oxazoline derivatives in high yields with up to 90:10 er. In addition, chiral cobalt (III) complexes catalyze the asymmetric intermolecular iodoacetalization of enol ethers with various alcohols to afford 3-iodoacetal derivatives in high yields with up to 92:8 er. Frontiers Media S.A. 2022-10-13 /pmc/articles/PMC9606352/ /pubmed/36311431 http://dx.doi.org/10.3389/fchem.2022.1034291 Text en Copyright © 2022 Salem and Takizawa. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Chemistry
Salem, Mohamed S. H.
Takizawa, Shinobu
New anionic cobalt(III) complexes enable enantioselective synthesis of spiro-fused oxazoline and iodoacetal derivatives
title New anionic cobalt(III) complexes enable enantioselective synthesis of spiro-fused oxazoline and iodoacetal derivatives
title_full New anionic cobalt(III) complexes enable enantioselective synthesis of spiro-fused oxazoline and iodoacetal derivatives
title_fullStr New anionic cobalt(III) complexes enable enantioselective synthesis of spiro-fused oxazoline and iodoacetal derivatives
title_full_unstemmed New anionic cobalt(III) complexes enable enantioselective synthesis of spiro-fused oxazoline and iodoacetal derivatives
title_short New anionic cobalt(III) complexes enable enantioselective synthesis of spiro-fused oxazoline and iodoacetal derivatives
title_sort new anionic cobalt(iii) complexes enable enantioselective synthesis of spiro-fused oxazoline and iodoacetal derivatives
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9606352/
https://www.ncbi.nlm.nih.gov/pubmed/36311431
http://dx.doi.org/10.3389/fchem.2022.1034291
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