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Non-Precious Metals Catalyze Formal [4 + 2] Cycloaddition Reactions of 1,2-Diazines and Siloxyalkynes under Ambient Conditions
[Image: see text] Copper(I) and nickel(0) complexes catalyze the formal [4 + 2] cycloaddition reactions of 1,2-diazines and siloxyalkynes, a reaction hitherto best catalyzed by silver salts. These catalysts based on earth abundant metals are not only competent, but the copper catalyst, in particular...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4076001/ https://www.ncbi.nlm.nih.gov/pubmed/24911346 http://dx.doi.org/10.1021/ol501254h |
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author | Sumaria, Chintan S. Türkmen, Yunus E. Rawal, Viresh H. |
author_facet | Sumaria, Chintan S. Türkmen, Yunus E. Rawal, Viresh H. |
author_sort | Sumaria, Chintan S. |
collection | PubMed |
description | [Image: see text] Copper(I) and nickel(0) complexes catalyze the formal [4 + 2] cycloaddition reactions of 1,2-diazines and siloxyalkynes, a reaction hitherto best catalyzed by silver salts. These catalysts based on earth abundant metals are not only competent, but the copper catalyst, in particular, promotes cycloadditions of pyrido[2,3-d]pyridazine and pyrido[3,4-d]pyridazine, enabling a new synthesis of quinoline and isoquinoline derivatives, as well as the formal [2 + 2] cycloaddition reaction of cyclohexenone with a siloxyalkyne. |
format | Online Article Text |
id | pubmed-4076001 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-40760012015-06-09 Non-Precious Metals Catalyze Formal [4 + 2] Cycloaddition Reactions of 1,2-Diazines and Siloxyalkynes under Ambient Conditions Sumaria, Chintan S. Türkmen, Yunus E. Rawal, Viresh H. Org Lett [Image: see text] Copper(I) and nickel(0) complexes catalyze the formal [4 + 2] cycloaddition reactions of 1,2-diazines and siloxyalkynes, a reaction hitherto best catalyzed by silver salts. These catalysts based on earth abundant metals are not only competent, but the copper catalyst, in particular, promotes cycloadditions of pyrido[2,3-d]pyridazine and pyrido[3,4-d]pyridazine, enabling a new synthesis of quinoline and isoquinoline derivatives, as well as the formal [2 + 2] cycloaddition reaction of cyclohexenone with a siloxyalkyne. American Chemical Society 2014-06-09 2014-06-20 /pmc/articles/PMC4076001/ /pubmed/24911346 http://dx.doi.org/10.1021/ol501254h Text en Copyright © 2014 American Chemical Society Terms of Use (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) |
spellingShingle | Sumaria, Chintan S. Türkmen, Yunus E. Rawal, Viresh H. Non-Precious Metals Catalyze Formal [4 + 2] Cycloaddition Reactions of 1,2-Diazines and Siloxyalkynes under Ambient Conditions |
title | Non-Precious Metals Catalyze Formal [4 + 2] Cycloaddition
Reactions of 1,2-Diazines and Siloxyalkynes under Ambient Conditions |
title_full | Non-Precious Metals Catalyze Formal [4 + 2] Cycloaddition
Reactions of 1,2-Diazines and Siloxyalkynes under Ambient Conditions |
title_fullStr | Non-Precious Metals Catalyze Formal [4 + 2] Cycloaddition
Reactions of 1,2-Diazines and Siloxyalkynes under Ambient Conditions |
title_full_unstemmed | Non-Precious Metals Catalyze Formal [4 + 2] Cycloaddition
Reactions of 1,2-Diazines and Siloxyalkynes under Ambient Conditions |
title_short | Non-Precious Metals Catalyze Formal [4 + 2] Cycloaddition
Reactions of 1,2-Diazines and Siloxyalkynes under Ambient Conditions |
title_sort | non-precious metals catalyze formal [4 + 2] cycloaddition
reactions of 1,2-diazines and siloxyalkynes under ambient conditions |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4076001/ https://www.ncbi.nlm.nih.gov/pubmed/24911346 http://dx.doi.org/10.1021/ol501254h |
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