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Catalytic Asymmetric Nitro-Mannich Reactions with a Yb/K Heterobimetallic Catalyst
A catalytic asymmetric nitro-Mannich (aza-Henry) reaction with rare earth metal/alkali metal heterobimetallic catalysts is described. A Yb/K heterobimetallic catalyst assembled by an amide-based ligand promoted the asymmetric nitro-Mannich reaction to afford enantioenriched anti-β-nitroamines in up...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257270/ https://www.ncbi.nlm.nih.gov/pubmed/20335980 http://dx.doi.org/10.3390/molecules15031280 |
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author | Nitabaru, Tatsuya Kumagai, Naoya Shibasaki, Masakatsu |
author_facet | Nitabaru, Tatsuya Kumagai, Naoya Shibasaki, Masakatsu |
author_sort | Nitabaru, Tatsuya |
collection | PubMed |
description | A catalytic asymmetric nitro-Mannich (aza-Henry) reaction with rare earth metal/alkali metal heterobimetallic catalysts is described. A Yb/K heterobimetallic catalyst assembled by an amide-based ligand promoted the asymmetric nitro-Mannich reaction to afford enantioenriched anti-β-nitroamines in up to 86% ee. Facile reduction of the nitro functionality allowed for efficient access to optically active 1,2-diamines. |
format | Online Article Text |
id | pubmed-6257270 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Molecular Diversity Preservation International |
record_format | MEDLINE/PubMed |
spelling | pubmed-62572702018-12-04 Catalytic Asymmetric Nitro-Mannich Reactions with a Yb/K Heterobimetallic Catalyst Nitabaru, Tatsuya Kumagai, Naoya Shibasaki, Masakatsu Molecules Article A catalytic asymmetric nitro-Mannich (aza-Henry) reaction with rare earth metal/alkali metal heterobimetallic catalysts is described. A Yb/K heterobimetallic catalyst assembled by an amide-based ligand promoted the asymmetric nitro-Mannich reaction to afford enantioenriched anti-β-nitroamines in up to 86% ee. Facile reduction of the nitro functionality allowed for efficient access to optically active 1,2-diamines. Molecular Diversity Preservation International 2010-03-04 /pmc/articles/PMC6257270/ /pubmed/20335980 http://dx.doi.org/10.3390/molecules15031280 Text en © 2010 by the authors; http://creativecommons.org/licenses/by/3.0/ licensee Molecular Diversity Preservation International, Basel, Switzerland. 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 Nitabaru, Tatsuya Kumagai, Naoya Shibasaki, Masakatsu Catalytic Asymmetric Nitro-Mannich Reactions with a Yb/K Heterobimetallic Catalyst |
title | Catalytic Asymmetric Nitro-Mannich Reactions with a Yb/K Heterobimetallic Catalyst |
title_full | Catalytic Asymmetric Nitro-Mannich Reactions with a Yb/K Heterobimetallic Catalyst |
title_fullStr | Catalytic Asymmetric Nitro-Mannich Reactions with a Yb/K Heterobimetallic Catalyst |
title_full_unstemmed | Catalytic Asymmetric Nitro-Mannich Reactions with a Yb/K Heterobimetallic Catalyst |
title_short | Catalytic Asymmetric Nitro-Mannich Reactions with a Yb/K Heterobimetallic Catalyst |
title_sort | catalytic asymmetric nitro-mannich reactions with a yb/k heterobimetallic catalyst |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257270/ https://www.ncbi.nlm.nih.gov/pubmed/20335980 http://dx.doi.org/10.3390/molecules15031280 |
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