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A truly green synthesis of α-aminonitriles via Strecker reaction

BACKGROUND: The classical Strecker reaction is one of the simplest and most economical methods for the synthesis of racemic α-aminonitriles (precursor of α-amino acids) and pharmacologically useful compounds. RESULTS: Indium powder in water is shown to act as a very efficient catalyst for one-pot, t...

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Detalles Bibliográficos
Autores principales: Bandyopadhyay, Debasish, Velazquez, Juliana M, Banik, Bimal K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3339329/
https://www.ncbi.nlm.nih.gov/pubmed/22373109
http://dx.doi.org/10.1186/2191-2858-1-11
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author Bandyopadhyay, Debasish
Velazquez, Juliana M
Banik, Bimal K
author_facet Bandyopadhyay, Debasish
Velazquez, Juliana M
Banik, Bimal K
author_sort Bandyopadhyay, Debasish
collection PubMed
description BACKGROUND: The classical Strecker reaction is one of the simplest and most economical methods for the synthesis of racemic α-aminonitriles (precursor of α-amino acids) and pharmacologically useful compounds. RESULTS: Indium powder in water is shown to act as a very efficient catalyst for one-pot, three-component synthesis of α-aminonitriles from diverse amines, aldehydes and TMSCN. This general rapid method is applicable to a wide range of amines and aldehydes and produces products in excellent yield. CONCLUSIONS: The present one-pot, three-component environmentally benign procedure for the synthesis of α-aminonitriles will find application in the synthesis of complex biologically active molecules.
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spelling pubmed-33393292012-04-30 A truly green synthesis of α-aminonitriles via Strecker reaction Bandyopadhyay, Debasish Velazquez, Juliana M Banik, Bimal K Org Med Chem Lett Original BACKGROUND: The classical Strecker reaction is one of the simplest and most economical methods for the synthesis of racemic α-aminonitriles (precursor of α-amino acids) and pharmacologically useful compounds. RESULTS: Indium powder in water is shown to act as a very efficient catalyst for one-pot, three-component synthesis of α-aminonitriles from diverse amines, aldehydes and TMSCN. This general rapid method is applicable to a wide range of amines and aldehydes and produces products in excellent yield. CONCLUSIONS: The present one-pot, three-component environmentally benign procedure for the synthesis of α-aminonitriles will find application in the synthesis of complex biologically active molecules. Springer 2011-10-04 /pmc/articles/PMC3339329/ /pubmed/22373109 http://dx.doi.org/10.1186/2191-2858-1-11 Text en Copyright © 2011 Bandyopadhyay et al; licensee Springer. https://creativecommons.org/licenses/by/2.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0 (https://creativecommons.org/licenses/by/2.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original
Bandyopadhyay, Debasish
Velazquez, Juliana M
Banik, Bimal K
A truly green synthesis of α-aminonitriles via Strecker reaction
title A truly green synthesis of α-aminonitriles via Strecker reaction
title_full A truly green synthesis of α-aminonitriles via Strecker reaction
title_fullStr A truly green synthesis of α-aminonitriles via Strecker reaction
title_full_unstemmed A truly green synthesis of α-aminonitriles via Strecker reaction
title_short A truly green synthesis of α-aminonitriles via Strecker reaction
title_sort truly green synthesis of α-aminonitriles via strecker reaction
topic Original
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3339329/
https://www.ncbi.nlm.nih.gov/pubmed/22373109
http://dx.doi.org/10.1186/2191-2858-1-11
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