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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... Full description

Journal Title: Molecules (Basel Switzerland), May 24, 2013, Vol.18(6), pp.6173-6192
Main Author: Doháňošová, Jana
Other Authors: Gracza, Tibor
Format: Electronic Article Electronic Article
Language: English
Subjects:
ID: E-ISSN: 1420-3049 ; DOI: 10.3390/molecules18066173
Link: http://search.proquest.com/docview/1356394235/?pq-origsite=primo
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recordid: proquest1356394235
title: Asymmetric palladium-catalysed intramolecular Wacker-type cyclisations of unsaturated alcohols and amino alcohols.
format: Article
creator:
  • Doháňošová, Jana
  • Gracza, Tibor
subjects:
  • Alcohols–Chemistry
  • Amino Alcohols–Chemistry
  • Catalysis–Chemistry
  • Cyclization–Chemistry
  • Heterocyclic Compounds–Chemistry
  • Molecular Structure–Chemistry
  • Oxidation-Reduction–Chemistry
  • Oxidative Coupling–Chemistry
  • Palladium–Chemistry
  • Alcohols
  • Amino Alcohols
  • Heterocyclic Compounds
  • Palladium
ispartof: Molecules (Basel, Switzerland), May 24, 2013, Vol.18(6), pp.6173-6192
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.
language: eng
source:
identifier: E-ISSN: 1420-3049 ; DOI: 10.3390/molecules18066173
fulltext: fulltext
issn:
  • 14203049
  • 1420-3049
url: Link


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titleAsymmetric palladium-catalysed intramolecular Wacker-type cyclisations of unsaturated alcohols and amino alcohols.
creatorDoháňošová, Jana ; Gracza, Tibor
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identifierE-ISSN: 1420-3049 ; DOI: 10.3390/molecules18066173
subjectAlcohols–Chemistry ; Amino Alcohols–Chemistry ; Catalysis–Chemistry ; Cyclization–Chemistry ; Heterocyclic Compounds–Chemistry ; Molecular Structure–Chemistry ; Oxidation-Reduction–Chemistry ; Oxidative Coupling–Chemistry ; Palladium–Chemistry ; Alcohols ; Amino Alcohols ; Heterocyclic Compounds ; Palladium
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descriptionThe 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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