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Chiral phase-transfer catalysis in the asymmetric α-heterofunctionalization of prochiral nucleophiles

Chiral phase-transfer catalysis is one of the major catalytic principles in asymmetric catalysis. A broad variety of different catalysts and their use for challenging applications have been reported over the last decades. Besides asymmetric C–C bond forming reactions the use of chiral phase-transfer...

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Detalles Bibliográficos
Autores principales: Schörgenhumer, Johannes, Tiffner, Maximilian, Waser, Mario
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5588627/
https://www.ncbi.nlm.nih.gov/pubmed/28904619
http://dx.doi.org/10.3762/bjoc.13.170
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author Schörgenhumer, Johannes
Tiffner, Maximilian
Waser, Mario
author_facet Schörgenhumer, Johannes
Tiffner, Maximilian
Waser, Mario
author_sort Schörgenhumer, Johannes
collection PubMed
description Chiral phase-transfer catalysis is one of the major catalytic principles in asymmetric catalysis. A broad variety of different catalysts and their use for challenging applications have been reported over the last decades. Besides asymmetric C–C bond forming reactions the use of chiral phase-transfer catalysts for enantioselective α-heterofunctionalization reactions of prochiral nucleophiles became one of the most important field of application of this catalytic principle. Based on several highly spectacular recent reports, we thus wish to discuss some of the most important achievements in this field within the context of this review.
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spelling pubmed-55886272017-09-13 Chiral phase-transfer catalysis in the asymmetric α-heterofunctionalization of prochiral nucleophiles Schörgenhumer, Johannes Tiffner, Maximilian Waser, Mario Beilstein J Org Chem Review Chiral phase-transfer catalysis is one of the major catalytic principles in asymmetric catalysis. A broad variety of different catalysts and their use for challenging applications have been reported over the last decades. Besides asymmetric C–C bond forming reactions the use of chiral phase-transfer catalysts for enantioselective α-heterofunctionalization reactions of prochiral nucleophiles became one of the most important field of application of this catalytic principle. Based on several highly spectacular recent reports, we thus wish to discuss some of the most important achievements in this field within the context of this review. Beilstein-Institut 2017-08-22 /pmc/articles/PMC5588627/ /pubmed/28904619 http://dx.doi.org/10.3762/bjoc.13.170 Text en Copyright © 2017, Schörgenhumer et al. https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Review
Schörgenhumer, Johannes
Tiffner, Maximilian
Waser, Mario
Chiral phase-transfer catalysis in the asymmetric α-heterofunctionalization of prochiral nucleophiles
title Chiral phase-transfer catalysis in the asymmetric α-heterofunctionalization of prochiral nucleophiles
title_full Chiral phase-transfer catalysis in the asymmetric α-heterofunctionalization of prochiral nucleophiles
title_fullStr Chiral phase-transfer catalysis in the asymmetric α-heterofunctionalization of prochiral nucleophiles
title_full_unstemmed Chiral phase-transfer catalysis in the asymmetric α-heterofunctionalization of prochiral nucleophiles
title_short Chiral phase-transfer catalysis in the asymmetric α-heterofunctionalization of prochiral nucleophiles
title_sort chiral phase-transfer catalysis in the asymmetric α-heterofunctionalization of prochiral nucleophiles
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5588627/
https://www.ncbi.nlm.nih.gov/pubmed/28904619
http://dx.doi.org/10.3762/bjoc.13.170
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