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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2018
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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. |
format | Online Article Text |
id | pubmed-5903423 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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
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title_full | Diastereo- and enantioselective additions of α-nitro esters to imines for anti-α,β-diamino acid synthesis with α-alkyl-substitution
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title_fullStr | Diastereo- and enantioselective additions of α-nitro esters to imines for anti-α,β-diamino acid synthesis with α-alkyl-substitution
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title_full_unstemmed | Diastereo- and enantioselective additions of α-nitro esters to imines for anti-α,β-diamino acid synthesis with α-alkyl-substitution
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title_short | Diastereo- and enantioselective additions of α-nitro esters to imines for anti-α,β-diamino acid synthesis with α-alkyl-substitution
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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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