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Diastereo- and enantioselective additions of α-nitro esters to imines for anti-α,β-diamino acid synthesis with α-alkyl-substitution

The discovery that a C(2)-symmetric bis(AMidine) [BAM] catalyst promotes an anti-selective addition of α-substituted α-nitro esters to imines is described, providing α-substituted α,β-diamino ester products with high diastereo- and enantioselectivity. When compared to the function of a BAM catalyst...

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Detalles Bibliográficos
Autores principales: Sprague, Daniel J., Singh, Anand, Johnston, Jeffrey N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5903423/
https://www.ncbi.nlm.nih.gov/pubmed/29719706
http://dx.doi.org/10.1039/c7sc05176j
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author Sprague, Daniel J.
Singh, Anand
Johnston, Jeffrey N.
author_facet Sprague, Daniel J.
Singh, Anand
Johnston, Jeffrey N.
author_sort Sprague, Daniel J.
collection PubMed
description The discovery that a C(2)-symmetric bis(AMidine) [BAM] catalyst promotes an anti-selective addition of α-substituted α-nitro esters to imines is described, providing α-substituted α,β-diamino ester products with high diastereo- and enantioselectivity. When compared to the function of a BAM catalyst reported previously, the pair offer a rare example of diastereodivergence using a bifunctional Brønsted acid–base organocatalyst.
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spelling pubmed-59034232018-05-01 Diastereo- and enantioselective additions of α-nitro esters to imines for anti-α,β-diamino acid synthesis with α-alkyl-substitution Sprague, Daniel J. Singh, Anand Johnston, Jeffrey N. Chem Sci Chemistry The discovery that a C(2)-symmetric bis(AMidine) [BAM] catalyst promotes an anti-selective addition of α-substituted α-nitro esters to imines is described, providing α-substituted α,β-diamino ester products with high diastereo- and enantioselectivity. When compared to the function of a BAM catalyst reported previously, the pair offer a rare example of diastereodivergence using a bifunctional Brønsted acid–base organocatalyst. Royal Society of Chemistry 2018-01-31 /pmc/articles/PMC5903423/ /pubmed/29719706 http://dx.doi.org/10.1039/c7sc05176j Text en This journal is © The Royal Society of Chemistry 2018 http://creativecommons.org/licenses/by/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0)
spellingShingle Chemistry
Sprague, Daniel J.
Singh, Anand
Johnston, Jeffrey N.
Diastereo- and enantioselective additions of α-nitro esters to imines for anti-α,β-diamino acid synthesis with α-alkyl-substitution
title Diastereo- and enantioselective additions of α-nitro esters to imines for anti-α,β-diamino acid synthesis with α-alkyl-substitution
title_full Diastereo- and enantioselective additions of α-nitro esters to imines for anti-α,β-diamino acid synthesis with α-alkyl-substitution
title_fullStr Diastereo- and enantioselective additions of α-nitro esters to imines for anti-α,β-diamino acid synthesis with α-alkyl-substitution
title_full_unstemmed Diastereo- and enantioselective additions of α-nitro esters to imines for anti-α,β-diamino acid synthesis with α-alkyl-substitution
title_short Diastereo- and enantioselective additions of α-nitro esters to imines for anti-α,β-diamino acid synthesis with α-alkyl-substitution
title_sort diastereo- and enantioselective additions of α-nitro esters to imines for anti-α,β-diamino acid synthesis with α-alkyl-substitution
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5903423/
https://www.ncbi.nlm.nih.gov/pubmed/29719706
http://dx.doi.org/10.1039/c7sc05176j
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