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The Asymmetric A(3)(Aldehyde–Alkyne–Amine) Coupling: Highly Enantioselective Access to Propargylamines
The recent developments in asymmetric A(3) (aldehyde–alkyne–amine) coupling has been summarized in this review. Several interesting modifications of the ligands enabled the highly enantioselective synthesis of chiral propargylamines, which are further used in the construction of nitrogen-containing...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6480255/ https://www.ncbi.nlm.nih.gov/pubmed/30925732 http://dx.doi.org/10.3390/molecules24071216 |
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author | Mo, Jia-Nan Su, Junqi Zhao, Jiannan |
author_facet | Mo, Jia-Nan Su, Junqi Zhao, Jiannan |
author_sort | Mo, Jia-Nan |
collection | PubMed |
description | The recent developments in asymmetric A(3) (aldehyde–alkyne–amine) coupling has been summarized in this review. Several interesting modifications of the ligands enabled the highly enantioselective synthesis of chiral propargylamines, which are further used in the construction of nitrogen-containing chiral building blocks. |
format | Online Article Text |
id | pubmed-6480255 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-64802552019-04-30 The Asymmetric A(3)(Aldehyde–Alkyne–Amine) Coupling: Highly Enantioselective Access to Propargylamines Mo, Jia-Nan Su, Junqi Zhao, Jiannan Molecules Review The recent developments in asymmetric A(3) (aldehyde–alkyne–amine) coupling has been summarized in this review. Several interesting modifications of the ligands enabled the highly enantioselective synthesis of chiral propargylamines, which are further used in the construction of nitrogen-containing chiral building blocks. MDPI 2019-03-28 /pmc/articles/PMC6480255/ /pubmed/30925732 http://dx.doi.org/10.3390/molecules24071216 Text en © 2019 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 (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Mo, Jia-Nan Su, Junqi Zhao, Jiannan The Asymmetric A(3)(Aldehyde–Alkyne–Amine) Coupling: Highly Enantioselective Access to Propargylamines |
title | The Asymmetric A(3)(Aldehyde–Alkyne–Amine) Coupling: Highly Enantioselective Access to Propargylamines |
title_full | The Asymmetric A(3)(Aldehyde–Alkyne–Amine) Coupling: Highly Enantioselective Access to Propargylamines |
title_fullStr | The Asymmetric A(3)(Aldehyde–Alkyne–Amine) Coupling: Highly Enantioselective Access to Propargylamines |
title_full_unstemmed | The Asymmetric A(3)(Aldehyde–Alkyne–Amine) Coupling: Highly Enantioselective Access to Propargylamines |
title_short | The Asymmetric A(3)(Aldehyde–Alkyne–Amine) Coupling: Highly Enantioselective Access to Propargylamines |
title_sort | asymmetric a(3)(aldehyde–alkyne–amine) coupling: highly enantioselective access to propargylamines |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6480255/ https://www.ncbi.nlm.nih.gov/pubmed/30925732 http://dx.doi.org/10.3390/molecules24071216 |
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