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Multicomponent synthesis of substituted pyridines via a catalytic intermolecular aza-Wittig/Diels–Alder sequence

A three-component synthesis of polysubstituted pyridines has been developed, based upon the synthesis of 2-azadienes by a redox-neutral catalytic intermolecular aza-Wittig reaction and their subsequent Diels–Alder reactions. The two-pot process has been demonstrated using a range of aryl and heteroa...

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Detalles Bibliográficos
Autores principales: Bayana, Mary E., Wailes, J. Steven, Marsden, Stephen P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9477066/
https://www.ncbi.nlm.nih.gov/pubmed/36275096
http://dx.doi.org/10.1039/d2ra05018h
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author Bayana, Mary E.
Wailes, J. Steven
Marsden, Stephen P.
author_facet Bayana, Mary E.
Wailes, J. Steven
Marsden, Stephen P.
author_sort Bayana, Mary E.
collection PubMed
description A three-component synthesis of polysubstituted pyridines has been developed, based upon the synthesis of 2-azadienes by a redox-neutral catalytic intermolecular aza-Wittig reaction and their subsequent Diels–Alder reactions. The two-pot process has been demonstrated using a range of aryl and heteroaromatic aldehydes, substituted α,β-unsaturated acids and push–pull enamines, to give rapid access to diverse tri- and tetrasubstituted pyridines.
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spelling pubmed-94770662022-10-20 Multicomponent synthesis of substituted pyridines via a catalytic intermolecular aza-Wittig/Diels–Alder sequence Bayana, Mary E. Wailes, J. Steven Marsden, Stephen P. RSC Adv Chemistry A three-component synthesis of polysubstituted pyridines has been developed, based upon the synthesis of 2-azadienes by a redox-neutral catalytic intermolecular aza-Wittig reaction and their subsequent Diels–Alder reactions. The two-pot process has been demonstrated using a range of aryl and heteroaromatic aldehydes, substituted α,β-unsaturated acids and push–pull enamines, to give rapid access to diverse tri- and tetrasubstituted pyridines. The Royal Society of Chemistry 2022-09-15 /pmc/articles/PMC9477066/ /pubmed/36275096 http://dx.doi.org/10.1039/d2ra05018h Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Bayana, Mary E.
Wailes, J. Steven
Marsden, Stephen P.
Multicomponent synthesis of substituted pyridines via a catalytic intermolecular aza-Wittig/Diels–Alder sequence
title Multicomponent synthesis of substituted pyridines via a catalytic intermolecular aza-Wittig/Diels–Alder sequence
title_full Multicomponent synthesis of substituted pyridines via a catalytic intermolecular aza-Wittig/Diels–Alder sequence
title_fullStr Multicomponent synthesis of substituted pyridines via a catalytic intermolecular aza-Wittig/Diels–Alder sequence
title_full_unstemmed Multicomponent synthesis of substituted pyridines via a catalytic intermolecular aza-Wittig/Diels–Alder sequence
title_short Multicomponent synthesis of substituted pyridines via a catalytic intermolecular aza-Wittig/Diels–Alder sequence
title_sort multicomponent synthesis of substituted pyridines via a catalytic intermolecular aza-wittig/diels–alder sequence
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9477066/
https://www.ncbi.nlm.nih.gov/pubmed/36275096
http://dx.doi.org/10.1039/d2ra05018h
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