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Efficient synthesis of spirooxindolyl oxazol-2(5H)-ones via palladium(ii)-catalyzed addition of arylboronic acids to nitriles
A versatile synthesis of spirooxindolyl oxazol-2(5H)-ones via palladium(ii)-catalyzed addition of arylboronic acids to nitriles is described. A wide range of spirooxindolyl oxazol-2(5H)-ones and other spirocyclic frameworks incorporating the oxazol-2(5H)-one unit can be readily prepared in good to h...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9071805/ https://www.ncbi.nlm.nih.gov/pubmed/35528398 http://dx.doi.org/10.1039/c9ra07216k |
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author | Song, Hao Cheng, Na She, Li-Qin Wu, Yi Liao, Wei-Wei |
author_facet | Song, Hao Cheng, Na She, Li-Qin Wu, Yi Liao, Wei-Wei |
author_sort | Song, Hao |
collection | PubMed |
description | A versatile synthesis of spirooxindolyl oxazol-2(5H)-ones via palladium(ii)-catalyzed addition of arylboronic acids to nitriles is described. A wide range of spirooxindolyl oxazol-2(5H)-ones and other spirocyclic frameworks incorporating the oxazol-2(5H)-one unit can be readily prepared in good to high yields under the optimal conditions. |
format | Online Article Text |
id | pubmed-9071805 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90718052022-05-06 Efficient synthesis of spirooxindolyl oxazol-2(5H)-ones via palladium(ii)-catalyzed addition of arylboronic acids to nitriles Song, Hao Cheng, Na She, Li-Qin Wu, Yi Liao, Wei-Wei RSC Adv Chemistry A versatile synthesis of spirooxindolyl oxazol-2(5H)-ones via palladium(ii)-catalyzed addition of arylboronic acids to nitriles is described. A wide range of spirooxindolyl oxazol-2(5H)-ones and other spirocyclic frameworks incorporating the oxazol-2(5H)-one unit can be readily prepared in good to high yields under the optimal conditions. The Royal Society of Chemistry 2019-09-17 /pmc/articles/PMC9071805/ /pubmed/35528398 http://dx.doi.org/10.1039/c9ra07216k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Song, Hao Cheng, Na She, Li-Qin Wu, Yi Liao, Wei-Wei Efficient synthesis of spirooxindolyl oxazol-2(5H)-ones via palladium(ii)-catalyzed addition of arylboronic acids to nitriles |
title | Efficient synthesis of spirooxindolyl oxazol-2(5H)-ones via palladium(ii)-catalyzed addition of arylboronic acids to nitriles |
title_full | Efficient synthesis of spirooxindolyl oxazol-2(5H)-ones via palladium(ii)-catalyzed addition of arylboronic acids to nitriles |
title_fullStr | Efficient synthesis of spirooxindolyl oxazol-2(5H)-ones via palladium(ii)-catalyzed addition of arylboronic acids to nitriles |
title_full_unstemmed | Efficient synthesis of spirooxindolyl oxazol-2(5H)-ones via palladium(ii)-catalyzed addition of arylboronic acids to nitriles |
title_short | Efficient synthesis of spirooxindolyl oxazol-2(5H)-ones via palladium(ii)-catalyzed addition of arylboronic acids to nitriles |
title_sort | efficient synthesis of spirooxindolyl oxazol-2(5h)-ones via palladium(ii)-catalyzed addition of arylboronic acids to nitriles |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9071805/ https://www.ncbi.nlm.nih.gov/pubmed/35528398 http://dx.doi.org/10.1039/c9ra07216k |
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