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Rh(iii)-catalyzed synthesis of dibenzo[b,d]pyran-6-ones from aryl ketone O-acetyl oximes and quinones via C–H activation and C–C bond cleavage
A redox-neutral synthesis of dibenzo[b,d]pyran-6-ones from aryl ketone O-acetyl oximes and quinones has been realized via Rh(iii)-catalyzed cascade C–H activation annulation. A possible Rh(iii)–Rh(v)–Rh(iii) mechanism involving an unprecedented β-C elimination step was proposed.
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9096810/ https://www.ncbi.nlm.nih.gov/pubmed/35702227 http://dx.doi.org/10.1039/d2ra02074b |
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author | Yang, Wei Zhang, Haonan Liu, Yu Tang, Cuiman Xu, Xiaohui Liu, Jiaqi |
author_facet | Yang, Wei Zhang, Haonan Liu, Yu Tang, Cuiman Xu, Xiaohui Liu, Jiaqi |
author_sort | Yang, Wei |
collection | PubMed |
description | A redox-neutral synthesis of dibenzo[b,d]pyran-6-ones from aryl ketone O-acetyl oximes and quinones has been realized via Rh(iii)-catalyzed cascade C–H activation annulation. A possible Rh(iii)–Rh(v)–Rh(iii) mechanism involving an unprecedented β-C elimination step was proposed. |
format | Online Article Text |
id | pubmed-9096810 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90968102022-06-13 Rh(iii)-catalyzed synthesis of dibenzo[b,d]pyran-6-ones from aryl ketone O-acetyl oximes and quinones via C–H activation and C–C bond cleavage Yang, Wei Zhang, Haonan Liu, Yu Tang, Cuiman Xu, Xiaohui Liu, Jiaqi RSC Adv Chemistry A redox-neutral synthesis of dibenzo[b,d]pyran-6-ones from aryl ketone O-acetyl oximes and quinones has been realized via Rh(iii)-catalyzed cascade C–H activation annulation. A possible Rh(iii)–Rh(v)–Rh(iii) mechanism involving an unprecedented β-C elimination step was proposed. The Royal Society of Chemistry 2022-05-12 /pmc/articles/PMC9096810/ /pubmed/35702227 http://dx.doi.org/10.1039/d2ra02074b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Yang, Wei Zhang, Haonan Liu, Yu Tang, Cuiman Xu, Xiaohui Liu, Jiaqi Rh(iii)-catalyzed synthesis of dibenzo[b,d]pyran-6-ones from aryl ketone O-acetyl oximes and quinones via C–H activation and C–C bond cleavage |
title | Rh(iii)-catalyzed synthesis of dibenzo[b,d]pyran-6-ones from aryl ketone O-acetyl oximes and quinones via C–H activation and C–C bond cleavage |
title_full | Rh(iii)-catalyzed synthesis of dibenzo[b,d]pyran-6-ones from aryl ketone O-acetyl oximes and quinones via C–H activation and C–C bond cleavage |
title_fullStr | Rh(iii)-catalyzed synthesis of dibenzo[b,d]pyran-6-ones from aryl ketone O-acetyl oximes and quinones via C–H activation and C–C bond cleavage |
title_full_unstemmed | Rh(iii)-catalyzed synthesis of dibenzo[b,d]pyran-6-ones from aryl ketone O-acetyl oximes and quinones via C–H activation and C–C bond cleavage |
title_short | Rh(iii)-catalyzed synthesis of dibenzo[b,d]pyran-6-ones from aryl ketone O-acetyl oximes and quinones via C–H activation and C–C bond cleavage |
title_sort | rh(iii)-catalyzed synthesis of dibenzo[b,d]pyran-6-ones from aryl ketone o-acetyl oximes and quinones via c–h activation and c–c bond cleavage |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9096810/ https://www.ncbi.nlm.nih.gov/pubmed/35702227 http://dx.doi.org/10.1039/d2ra02074b |
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