Asymmetric Palladium-Catalysed Intramolecular Wacker-Type Cyclisations of Unsaturated Alcohols and Amino Alcohols

The palladium (II)-catalysed reactions of alkenols and aminoalkenols such as oxycarbonylations or bicyclisations are powerful methods for the construction of oxygen and nitrogen-containing heterocyclic compounds. This review highlights recent progress in the development of the asymmetric palladium(I...

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Detalles Bibliográficos
Autores principales: Doháňošová, Jana, Gracza, Tibor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2013
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270647/
https://www.ncbi.nlm.nih.gov/pubmed/23708231
http://dx.doi.org/10.3390/molecules18066173
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author Doháňošová, Jana
Gracza, Tibor
author_facet Doháňošová, Jana
Gracza, Tibor
author_sort Doháňošová, Jana
collection PubMed
description The palladium (II)-catalysed reactions of alkenols and aminoalkenols such as oxycarbonylations or bicyclisations are powerful methods for the construction of oxygen and nitrogen-containing heterocyclic compounds. This review highlights recent progress in the development of the asymmetric palladium(II)-catalysed Wacker-type cyclisations of unsaturated polyols and aminoalcohols. The scope, limitations, and applications of these reactions are presented.
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spelling pubmed-62706472018-12-17 Asymmetric Palladium-Catalysed Intramolecular Wacker-Type Cyclisations of Unsaturated Alcohols and Amino Alcohols Doháňošová, Jana Gracza, Tibor Molecules Review The palladium (II)-catalysed reactions of alkenols and aminoalkenols such as oxycarbonylations or bicyclisations are powerful methods for the construction of oxygen and nitrogen-containing heterocyclic compounds. This review highlights recent progress in the development of the asymmetric palladium(II)-catalysed Wacker-type cyclisations of unsaturated polyols and aminoalcohols. The scope, limitations, and applications of these reactions are presented. MDPI 2013-05-24 /pmc/articles/PMC6270647/ /pubmed/23708231 http://dx.doi.org/10.3390/molecules18066173 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Doháňošová, Jana
Gracza, Tibor
Asymmetric Palladium-Catalysed Intramolecular Wacker-Type Cyclisations of Unsaturated Alcohols and Amino Alcohols
title Asymmetric Palladium-Catalysed Intramolecular Wacker-Type Cyclisations of Unsaturated Alcohols and Amino Alcohols
title_full Asymmetric Palladium-Catalysed Intramolecular Wacker-Type Cyclisations of Unsaturated Alcohols and Amino Alcohols
title_fullStr Asymmetric Palladium-Catalysed Intramolecular Wacker-Type Cyclisations of Unsaturated Alcohols and Amino Alcohols
title_full_unstemmed Asymmetric Palladium-Catalysed Intramolecular Wacker-Type Cyclisations of Unsaturated Alcohols and Amino Alcohols
title_short Asymmetric Palladium-Catalysed Intramolecular Wacker-Type Cyclisations of Unsaturated Alcohols and Amino Alcohols
title_sort asymmetric palladium-catalysed intramolecular wacker-type cyclisations of unsaturated alcohols and amino alcohols
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270647/
https://www.ncbi.nlm.nih.gov/pubmed/23708231
http://dx.doi.org/10.3390/molecules18066173
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