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Towards Tartaric-Acid-Derived Asymmetric Organocatalysts

Tartaric acid is one of the most prominent naturally occurring chiral compounds. Whereas its application in the production of chiral ligands for metal-catalysed reactions has been exhaustively investigated, its potential to provide new organocatalysts has been less extensively explored. Nevertheless...

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Detalles Bibliográficos
Autores principales: Gratzer, Katharina, Gururaja, Guddeangadi N, Waser, Mario
Formato: Online Artículo Texto
Lenguaje:English
Publicado: WILEY-VCH Verlag 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3806311/
https://www.ncbi.nlm.nih.gov/pubmed/24194674
http://dx.doi.org/10.1002/ejoc.201201675
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author Gratzer, Katharina
Gururaja, Guddeangadi N
Waser, Mario
author_facet Gratzer, Katharina
Gururaja, Guddeangadi N
Waser, Mario
author_sort Gratzer, Katharina
collection PubMed
description Tartaric acid is one of the most prominent naturally occurring chiral compounds. Whereas its application in the production of chiral ligands for metal-catalysed reactions has been exhaustively investigated, its potential to provide new organocatalysts has been less extensively explored. Nevertheless, some impressive results, such as the use of TADDOLs as chiral H-bonding catalysts or of tartrate-derived asymmetric quaternary ammonium salt catalysts, have been reported over the last decade. The goal of this article is to provide a representative overview of the potential and the limitations of tartaric acid or TADDOLs in the creation of new organocatalysts and to highlight some of the most spectacular applications of these catalysts, as well as to summarize case studies in which other classes of chiral backbones were better suited.
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spelling pubmed-38063112013-11-03 Towards Tartaric-Acid-Derived Asymmetric Organocatalysts Gratzer, Katharina Gururaja, Guddeangadi N Waser, Mario European J Org Chem Microreview Tartaric acid is one of the most prominent naturally occurring chiral compounds. Whereas its application in the production of chiral ligands for metal-catalysed reactions has been exhaustively investigated, its potential to provide new organocatalysts has been less extensively explored. Nevertheless, some impressive results, such as the use of TADDOLs as chiral H-bonding catalysts or of tartrate-derived asymmetric quaternary ammonium salt catalysts, have been reported over the last decade. The goal of this article is to provide a representative overview of the potential and the limitations of tartaric acid or TADDOLs in the creation of new organocatalysts and to highlight some of the most spectacular applications of these catalysts, as well as to summarize case studies in which other classes of chiral backbones were better suited. WILEY-VCH Verlag 2013-07 2013-06-03 /pmc/articles/PMC3806311/ /pubmed/24194674 http://dx.doi.org/10.1002/ejoc.201201675 Text en Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.
spellingShingle Microreview
Gratzer, Katharina
Gururaja, Guddeangadi N
Waser, Mario
Towards Tartaric-Acid-Derived Asymmetric Organocatalysts
title Towards Tartaric-Acid-Derived Asymmetric Organocatalysts
title_full Towards Tartaric-Acid-Derived Asymmetric Organocatalysts
title_fullStr Towards Tartaric-Acid-Derived Asymmetric Organocatalysts
title_full_unstemmed Towards Tartaric-Acid-Derived Asymmetric Organocatalysts
title_short Towards Tartaric-Acid-Derived Asymmetric Organocatalysts
title_sort towards tartaric-acid-derived asymmetric organocatalysts
topic Microreview
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3806311/
https://www.ncbi.nlm.nih.gov/pubmed/24194674
http://dx.doi.org/10.1002/ejoc.201201675
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