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PtO(2)/PTSA system catalyzed regioselective hydration of internal arylalkynes bearing electron withdrawing groups
A highly efficient PtO(2)/PTSA catalyst system for the hydration of a wide array of alkynes was developed. This method proved to be compatible with a large range of functional groups and the ketone products were obtained in high yields. The scope of this methodology was also extended to the synthesi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9079276/ https://www.ncbi.nlm.nih.gov/pubmed/35542815 http://dx.doi.org/10.1039/c8ra00564h |
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author | Lin, Hsin-Ping Ibrahim, Nada Provot, Olivier Alami, Mouad Hamze, Abdallah |
author_facet | Lin, Hsin-Ping Ibrahim, Nada Provot, Olivier Alami, Mouad Hamze, Abdallah |
author_sort | Lin, Hsin-Ping |
collection | PubMed |
description | A highly efficient PtO(2)/PTSA catalyst system for the hydration of a wide array of alkynes was developed. This method proved to be compatible with a large range of functional groups and the ketone products were obtained in high yields. The scope of this methodology was also extended to the synthesis of 3-aryl-isochromenones, -indoles and -benzofurans. |
format | Online Article Text |
id | pubmed-9079276 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90792762022-05-09 PtO(2)/PTSA system catalyzed regioselective hydration of internal arylalkynes bearing electron withdrawing groups Lin, Hsin-Ping Ibrahim, Nada Provot, Olivier Alami, Mouad Hamze, Abdallah RSC Adv Chemistry A highly efficient PtO(2)/PTSA catalyst system for the hydration of a wide array of alkynes was developed. This method proved to be compatible with a large range of functional groups and the ketone products were obtained in high yields. The scope of this methodology was also extended to the synthesis of 3-aryl-isochromenones, -indoles and -benzofurans. The Royal Society of Chemistry 2018-03-23 /pmc/articles/PMC9079276/ /pubmed/35542815 http://dx.doi.org/10.1039/c8ra00564h Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Lin, Hsin-Ping Ibrahim, Nada Provot, Olivier Alami, Mouad Hamze, Abdallah PtO(2)/PTSA system catalyzed regioselective hydration of internal arylalkynes bearing electron withdrawing groups |
title | PtO(2)/PTSA system catalyzed regioselective hydration of internal arylalkynes bearing electron withdrawing groups |
title_full | PtO(2)/PTSA system catalyzed regioselective hydration of internal arylalkynes bearing electron withdrawing groups |
title_fullStr | PtO(2)/PTSA system catalyzed regioselective hydration of internal arylalkynes bearing electron withdrawing groups |
title_full_unstemmed | PtO(2)/PTSA system catalyzed regioselective hydration of internal arylalkynes bearing electron withdrawing groups |
title_short | PtO(2)/PTSA system catalyzed regioselective hydration of internal arylalkynes bearing electron withdrawing groups |
title_sort | pto(2)/ptsa system catalyzed regioselective hydration of internal arylalkynes bearing electron withdrawing groups |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9079276/ https://www.ncbi.nlm.nih.gov/pubmed/35542815 http://dx.doi.org/10.1039/c8ra00564h |
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