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Oxidative dearomatic approach towards the synthesis of erythrina skeleton: a formal synthesis of demethoxyerythratidinone
A concise synthetic route leading to highly functional erythrina alkaloid skeletons has been developed. The key process is an oxidative carbon-carbon coupling followed by a conjugated addition. Based on this new strategy, a formal synthesis of demethoxyerythratidinone was completed in only 6 steps f...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4131647/ http://dx.doi.org/10.1007/s13659-011-0045-1 |
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author | Pan, Zhi-Qiang Liang, Ji-Xuan Chen, Jing-Bo Yang, Xiao-Dong Zhang, Hong-Bin |
author_facet | Pan, Zhi-Qiang Liang, Ji-Xuan Chen, Jing-Bo Yang, Xiao-Dong Zhang, Hong-Bin |
author_sort | Pan, Zhi-Qiang |
collection | PubMed |
description | A concise synthetic route leading to highly functional erythrina alkaloid skeletons has been developed. The key process is an oxidative carbon-carbon coupling followed by a conjugated addition. Based on this new strategy, a formal synthesis of demethoxyerythratidinone was completed in only 6 steps from 4-aminophenol. [Image: see text] |
format | Online Article Text |
id | pubmed-4131647 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-41316472014-08-20 Oxidative dearomatic approach towards the synthesis of erythrina skeleton: a formal synthesis of demethoxyerythratidinone Pan, Zhi-Qiang Liang, Ji-Xuan Chen, Jing-Bo Yang, Xiao-Dong Zhang, Hong-Bin Nat Prod Bioprospect Regular Article A concise synthetic route leading to highly functional erythrina alkaloid skeletons has been developed. The key process is an oxidative carbon-carbon coupling followed by a conjugated addition. Based on this new strategy, a formal synthesis of demethoxyerythratidinone was completed in only 6 steps from 4-aminophenol. [Image: see text] Springer Berlin Heidelberg 2011-12-23 /pmc/articles/PMC4131647/ http://dx.doi.org/10.1007/s13659-011-0045-1 Text en © The Author(s) 2011 https://creativecommons.org/licenses/by/4.0/ This article is published under license to BioMed Central Ltd. Open Access This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Regular Article Pan, Zhi-Qiang Liang, Ji-Xuan Chen, Jing-Bo Yang, Xiao-Dong Zhang, Hong-Bin Oxidative dearomatic approach towards the synthesis of erythrina skeleton: a formal synthesis of demethoxyerythratidinone |
title | Oxidative dearomatic approach towards the synthesis of erythrina skeleton: a formal synthesis of demethoxyerythratidinone |
title_full | Oxidative dearomatic approach towards the synthesis of erythrina skeleton: a formal synthesis of demethoxyerythratidinone |
title_fullStr | Oxidative dearomatic approach towards the synthesis of erythrina skeleton: a formal synthesis of demethoxyerythratidinone |
title_full_unstemmed | Oxidative dearomatic approach towards the synthesis of erythrina skeleton: a formal synthesis of demethoxyerythratidinone |
title_short | Oxidative dearomatic approach towards the synthesis of erythrina skeleton: a formal synthesis of demethoxyerythratidinone |
title_sort | oxidative dearomatic approach towards the synthesis of erythrina skeleton: a formal synthesis of demethoxyerythratidinone |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4131647/ http://dx.doi.org/10.1007/s13659-011-0045-1 |
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