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Facile access to chiral γ-butyrolactones via rhodium-catalysed asymmetric hydrogenation of γ-butenolides and γ-hydroxybutenolides
The highly efficient Rh/ZhaoPhos-catalysed asymmetric hydrogenation of γ-butenolides and γ-hydroxybutenolides was successfully developed. This protocol provides an efficient and practical approach to the synthesis of various chiral γ-butyrolactones, which are synthetically valuable building blocks o...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10171041/ https://www.ncbi.nlm.nih.gov/pubmed/37181773 http://dx.doi.org/10.1039/d3sc00491k |
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author | Zhou, Yuxuan Guo, Siyuan Huang, Qiyuan Lang, Qiwei Chen, Gen-Qiang Zhang, Xumu |
author_facet | Zhou, Yuxuan Guo, Siyuan Huang, Qiyuan Lang, Qiwei Chen, Gen-Qiang Zhang, Xumu |
author_sort | Zhou, Yuxuan |
collection | PubMed |
description | The highly efficient Rh/ZhaoPhos-catalysed asymmetric hydrogenation of γ-butenolides and γ-hydroxybutenolides was successfully developed. This protocol provides an efficient and practical approach to the synthesis of various chiral γ-butyrolactones, which are synthetically valuable building blocks of diverse natural products and therapeutic substances, with excellent results (up to >99% conversion and 99% ee). Further follow-up transformations have been revealed to accomplish creative and efficient synthetic routes for several enantiomerically enriched drugs via this catalytic methodology. |
format | Online Article Text |
id | pubmed-10171041 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-101710412023-05-11 Facile access to chiral γ-butyrolactones via rhodium-catalysed asymmetric hydrogenation of γ-butenolides and γ-hydroxybutenolides Zhou, Yuxuan Guo, Siyuan Huang, Qiyuan Lang, Qiwei Chen, Gen-Qiang Zhang, Xumu Chem Sci Chemistry The highly efficient Rh/ZhaoPhos-catalysed asymmetric hydrogenation of γ-butenolides and γ-hydroxybutenolides was successfully developed. This protocol provides an efficient and practical approach to the synthesis of various chiral γ-butyrolactones, which are synthetically valuable building blocks of diverse natural products and therapeutic substances, with excellent results (up to >99% conversion and 99% ee). Further follow-up transformations have been revealed to accomplish creative and efficient synthetic routes for several enantiomerically enriched drugs via this catalytic methodology. The Royal Society of Chemistry 2023-04-15 /pmc/articles/PMC10171041/ /pubmed/37181773 http://dx.doi.org/10.1039/d3sc00491k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Zhou, Yuxuan Guo, Siyuan Huang, Qiyuan Lang, Qiwei Chen, Gen-Qiang Zhang, Xumu Facile access to chiral γ-butyrolactones via rhodium-catalysed asymmetric hydrogenation of γ-butenolides and γ-hydroxybutenolides |
title | Facile access to chiral γ-butyrolactones via rhodium-catalysed asymmetric hydrogenation of γ-butenolides and γ-hydroxybutenolides |
title_full | Facile access to chiral γ-butyrolactones via rhodium-catalysed asymmetric hydrogenation of γ-butenolides and γ-hydroxybutenolides |
title_fullStr | Facile access to chiral γ-butyrolactones via rhodium-catalysed asymmetric hydrogenation of γ-butenolides and γ-hydroxybutenolides |
title_full_unstemmed | Facile access to chiral γ-butyrolactones via rhodium-catalysed asymmetric hydrogenation of γ-butenolides and γ-hydroxybutenolides |
title_short | Facile access to chiral γ-butyrolactones via rhodium-catalysed asymmetric hydrogenation of γ-butenolides and γ-hydroxybutenolides |
title_sort | facile access to chiral γ-butyrolactones via rhodium-catalysed asymmetric hydrogenation of γ-butenolides and γ-hydroxybutenolides |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10171041/ https://www.ncbi.nlm.nih.gov/pubmed/37181773 http://dx.doi.org/10.1039/d3sc00491k |
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