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A Three-Component Reaction Forming Naphthyridones – Synthesis of Lophocladine Analogs
[Image: see text] A three-component reaction forming dihydro 2,7-naphthyridine-1-ones has been developed. These unstable dihydro intermediates can be either oxidized or reduced to form naphthyridones or tetrahydro naphthyridones, respectively. The reaction tolerates a large variety of aldehydes and...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3203621/ https://www.ncbi.nlm.nih.gov/pubmed/21879774 http://dx.doi.org/10.1021/ol202080x |
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author | Sellstedt, Magnus Almqvist, Fredrik |
author_facet | Sellstedt, Magnus Almqvist, Fredrik |
author_sort | Sellstedt, Magnus |
collection | PubMed |
description | [Image: see text] A three-component reaction forming dihydro 2,7-naphthyridine-1-ones has been developed. These unstable dihydro intermediates can be either oxidized or reduced to form naphthyridones or tetrahydro naphthyridones, respectively. The reaction tolerates a large variety of aldehydes and amines, and the produced compounds are analogs of the natural product lophocladine A. |
format | Online Article Text |
id | pubmed-3203621 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-32036212011-10-31 A Three-Component Reaction Forming Naphthyridones – Synthesis of Lophocladine Analogs Sellstedt, Magnus Almqvist, Fredrik Org Lett [Image: see text] A three-component reaction forming dihydro 2,7-naphthyridine-1-ones has been developed. These unstable dihydro intermediates can be either oxidized or reduced to form naphthyridones or tetrahydro naphthyridones, respectively. The reaction tolerates a large variety of aldehydes and amines, and the produced compounds are analogs of the natural product lophocladine A. American Chemical Society 2011-09-01 2011-10-07 /pmc/articles/PMC3203621/ /pubmed/21879774 http://dx.doi.org/10.1021/ol202080x Text en Copyright © 2011 American Chemical Society http://pubs.acs.org This is an open-access article distributed under the ACS AuthorChoice Terms & Conditions. Any use of this article, must conform to the terms of that license which are available at http://pubs.acs.org. |
spellingShingle | Sellstedt, Magnus Almqvist, Fredrik A Three-Component Reaction Forming Naphthyridones – Synthesis of Lophocladine Analogs |
title | A Three-Component Reaction Forming Naphthyridones – Synthesis of Lophocladine Analogs |
title_full | A Three-Component Reaction Forming Naphthyridones – Synthesis of Lophocladine Analogs |
title_fullStr | A Three-Component Reaction Forming Naphthyridones – Synthesis of Lophocladine Analogs |
title_full_unstemmed | A Three-Component Reaction Forming Naphthyridones – Synthesis of Lophocladine Analogs |
title_short | A Three-Component Reaction Forming Naphthyridones – Synthesis of Lophocladine Analogs |
title_sort | three-component reaction forming naphthyridones – synthesis of lophocladine analogs |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3203621/ https://www.ncbi.nlm.nih.gov/pubmed/21879774 http://dx.doi.org/10.1021/ol202080x |
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