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Efficient Preparation of α-Ketoacetals
The Weinreb amides 2a,b were prepared from the α,α-dimethoxyacetic acids 1c,d. A number of representative nucleophilic additions (RMgX and RLi) on 2 afforded α-ketoacetals 3a–j in 70–99% yield. These compounds represent a versatile arrangement of functional groups of significant synthetic value, as...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268805/ https://www.ncbi.nlm.nih.gov/pubmed/23174902 http://dx.doi.org/10.3390/molecules171213864 |
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author | Ayala-Mata, Francisco Barrera-Mendoza, Citlalli Jiménez-Vázquez, Hugo A. Vargas-Díaz, Elena Zepeda, L. Gerardo |
author_facet | Ayala-Mata, Francisco Barrera-Mendoza, Citlalli Jiménez-Vázquez, Hugo A. Vargas-Díaz, Elena Zepeda, L. Gerardo |
author_sort | Ayala-Mata, Francisco |
collection | PubMed |
description | The Weinreb amides 2a,b were prepared from the α,α-dimethoxyacetic acids 1c,d. A number of representative nucleophilic additions (RMgX and RLi) on 2 afforded α-ketoacetals 3a–j in 70–99% yield. These compounds represent a versatile arrangement of functional groups of significant synthetic value, as demonstrated in the synthesis of (±)-salbutamol. |
format | Online Article Text |
id | pubmed-6268805 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62688052018-12-14 Efficient Preparation of α-Ketoacetals Ayala-Mata, Francisco Barrera-Mendoza, Citlalli Jiménez-Vázquez, Hugo A. Vargas-Díaz, Elena Zepeda, L. Gerardo Molecules Article The Weinreb amides 2a,b were prepared from the α,α-dimethoxyacetic acids 1c,d. A number of representative nucleophilic additions (RMgX and RLi) on 2 afforded α-ketoacetals 3a–j in 70–99% yield. These compounds represent a versatile arrangement of functional groups of significant synthetic value, as demonstrated in the synthesis of (±)-salbutamol. MDPI 2012-11-22 /pmc/articles/PMC6268805/ /pubmed/23174902 http://dx.doi.org/10.3390/molecules171213864 Text en © 2012 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ 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 | Article Ayala-Mata, Francisco Barrera-Mendoza, Citlalli Jiménez-Vázquez, Hugo A. Vargas-Díaz, Elena Zepeda, L. Gerardo Efficient Preparation of α-Ketoacetals |
title | Efficient Preparation of α-Ketoacetals |
title_full | Efficient Preparation of α-Ketoacetals |
title_fullStr | Efficient Preparation of α-Ketoacetals |
title_full_unstemmed | Efficient Preparation of α-Ketoacetals |
title_short | Efficient Preparation of α-Ketoacetals |
title_sort | efficient preparation of α-ketoacetals |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268805/ https://www.ncbi.nlm.nih.gov/pubmed/23174902 http://dx.doi.org/10.3390/molecules171213864 |
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