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Synthesis of 2‐Alkynoates by Palladium(II)‐Catalyzed Oxidative Carbonylation of Terminal Alkynes and Alcohols

A homogeneous Pd(II) catalyst, utilizing a simple and inexpensive amine ligand (TMEDA), allows 2‐alkynoates to be prepared in high yields by an oxidative carbonylation of terminal alkynes and alcohols. The catalyst system overcomes many of the limitations of previous palladium carbonylation catalyst...

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Detalles Bibliográficos
Autores principales: Cao, Qun, Hughes, N. Louise, Muldoon, Mark J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5347984/
https://www.ncbi.nlm.nih.gov/pubmed/27305489
http://dx.doi.org/10.1002/chem.201602558
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author Cao, Qun
Hughes, N. Louise
Muldoon, Mark J.
author_facet Cao, Qun
Hughes, N. Louise
Muldoon, Mark J.
author_sort Cao, Qun
collection PubMed
description A homogeneous Pd(II) catalyst, utilizing a simple and inexpensive amine ligand (TMEDA), allows 2‐alkynoates to be prepared in high yields by an oxidative carbonylation of terminal alkynes and alcohols. The catalyst system overcomes many of the limitations of previous palladium carbonylation catalysts. It has an increased substrate scope, avoids large excesses of alcohol substrate and uses a desirable solvent. The catalyst employs oxygen as the terminal oxidant and can be operated under safer gas mixtures.
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spelling pubmed-53479842017-03-27 Synthesis of 2‐Alkynoates by Palladium(II)‐Catalyzed Oxidative Carbonylation of Terminal Alkynes and Alcohols Cao, Qun Hughes, N. Louise Muldoon, Mark J. Chemistry Communications A homogeneous Pd(II) catalyst, utilizing a simple and inexpensive amine ligand (TMEDA), allows 2‐alkynoates to be prepared in high yields by an oxidative carbonylation of terminal alkynes and alcohols. The catalyst system overcomes many of the limitations of previous palladium carbonylation catalysts. It has an increased substrate scope, avoids large excesses of alcohol substrate and uses a desirable solvent. The catalyst employs oxygen as the terminal oxidant and can be operated under safer gas mixtures. John Wiley and Sons Inc. 2016-07-19 2016-08-16 /pmc/articles/PMC5347984/ /pubmed/27305489 http://dx.doi.org/10.1002/chem.201602558 Text en © 2016 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Communications
Cao, Qun
Hughes, N. Louise
Muldoon, Mark J.
Synthesis of 2‐Alkynoates by Palladium(II)‐Catalyzed Oxidative Carbonylation of Terminal Alkynes and Alcohols
title Synthesis of 2‐Alkynoates by Palladium(II)‐Catalyzed Oxidative Carbonylation of Terminal Alkynes and Alcohols
title_full Synthesis of 2‐Alkynoates by Palladium(II)‐Catalyzed Oxidative Carbonylation of Terminal Alkynes and Alcohols
title_fullStr Synthesis of 2‐Alkynoates by Palladium(II)‐Catalyzed Oxidative Carbonylation of Terminal Alkynes and Alcohols
title_full_unstemmed Synthesis of 2‐Alkynoates by Palladium(II)‐Catalyzed Oxidative Carbonylation of Terminal Alkynes and Alcohols
title_short Synthesis of 2‐Alkynoates by Palladium(II)‐Catalyzed Oxidative Carbonylation of Terminal Alkynes and Alcohols
title_sort synthesis of 2‐alkynoates by palladium(ii)‐catalyzed oxidative carbonylation of terminal alkynes and alcohols
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5347984/
https://www.ncbi.nlm.nih.gov/pubmed/27305489
http://dx.doi.org/10.1002/chem.201602558
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