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Palladium-Catalyzed Intramolecular Cross-Dehydrogenative Coupling: Synthesis of Fused Imidazo[1,2-a]pyrimidines and Pyrazolo[1,5-a]pyrimidines
[Image: see text] A palladium-catalyzed intramolecular dehydrogenative coupling reaction was developed for the synthesis of fused imidazo[1,2-a]pyrimidines and pyrazolo[1,5-a]pyrimidines. The developed protocol provides a practical approach for the synthesis of biologically important substituted pyr...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641030/ https://www.ncbi.nlm.nih.gov/pubmed/31457205 http://dx.doi.org/10.1021/acsomega.6b00417 |
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author | Reddy Kotla, Siva K. Vandavasi, Jaya Kishore Wang, Jeh-Jeng Parang, Keykavous Tiwari, Rakesh K. |
author_facet | Reddy Kotla, Siva K. Vandavasi, Jaya Kishore Wang, Jeh-Jeng Parang, Keykavous Tiwari, Rakesh K. |
author_sort | Reddy Kotla, Siva K. |
collection | PubMed |
description | [Image: see text] A palladium-catalyzed intramolecular dehydrogenative coupling reaction was developed for the synthesis of fused imidazo[1,2-a]pyrimidines and pyrazolo[1,5-a]pyrimidines. The developed protocol provides a practical approach for the synthesis of biologically important substituted pyrimidines from easily available substrates, with a broad substrate scope under mild reaction conditions. |
format | Online Article Text |
id | pubmed-6641030 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-66410302019-08-27 Palladium-Catalyzed Intramolecular Cross-Dehydrogenative Coupling: Synthesis of Fused Imidazo[1,2-a]pyrimidines and Pyrazolo[1,5-a]pyrimidines Reddy Kotla, Siva K. Vandavasi, Jaya Kishore Wang, Jeh-Jeng Parang, Keykavous Tiwari, Rakesh K. ACS Omega [Image: see text] A palladium-catalyzed intramolecular dehydrogenative coupling reaction was developed for the synthesis of fused imidazo[1,2-a]pyrimidines and pyrazolo[1,5-a]pyrimidines. The developed protocol provides a practical approach for the synthesis of biologically important substituted pyrimidines from easily available substrates, with a broad substrate scope under mild reaction conditions. American Chemical Society 2017-01-04 /pmc/articles/PMC6641030/ /pubmed/31457205 http://dx.doi.org/10.1021/acsomega.6b00417 Text en Copyright © 2017 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Reddy Kotla, Siva K. Vandavasi, Jaya Kishore Wang, Jeh-Jeng Parang, Keykavous Tiwari, Rakesh K. Palladium-Catalyzed Intramolecular Cross-Dehydrogenative Coupling: Synthesis of Fused Imidazo[1,2-a]pyrimidines and Pyrazolo[1,5-a]pyrimidines |
title | Palladium-Catalyzed Intramolecular Cross-Dehydrogenative
Coupling: Synthesis of Fused
Imidazo[1,2-a]pyrimidines and Pyrazolo[1,5-a]pyrimidines |
title_full | Palladium-Catalyzed Intramolecular Cross-Dehydrogenative
Coupling: Synthesis of Fused
Imidazo[1,2-a]pyrimidines and Pyrazolo[1,5-a]pyrimidines |
title_fullStr | Palladium-Catalyzed Intramolecular Cross-Dehydrogenative
Coupling: Synthesis of Fused
Imidazo[1,2-a]pyrimidines and Pyrazolo[1,5-a]pyrimidines |
title_full_unstemmed | Palladium-Catalyzed Intramolecular Cross-Dehydrogenative
Coupling: Synthesis of Fused
Imidazo[1,2-a]pyrimidines and Pyrazolo[1,5-a]pyrimidines |
title_short | Palladium-Catalyzed Intramolecular Cross-Dehydrogenative
Coupling: Synthesis of Fused
Imidazo[1,2-a]pyrimidines and Pyrazolo[1,5-a]pyrimidines |
title_sort | palladium-catalyzed intramolecular cross-dehydrogenative
coupling: synthesis of fused
imidazo[1,2-a]pyrimidines and pyrazolo[1,5-a]pyrimidines |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641030/ https://www.ncbi.nlm.nih.gov/pubmed/31457205 http://dx.doi.org/10.1021/acsomega.6b00417 |
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