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Development of an enolate alkynylation approach towards the synthesis of the taiwanschirin natural products
Through the use of model studies, an approach was conceived towards the synthesis of the taiwanschirin family of natural products. These are structurally complex compounds which represent highly challenging and biologically active targets for total synthesis. This work describes a successful synthes...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8528008/ https://www.ncbi.nlm.nih.gov/pubmed/34777757 http://dx.doi.org/10.1039/d1sc04247e |
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author | Haughey, Maxwell B. Christensen, Kirsten E. Poole, Darren L. Donohoe, Timothy J. |
author_facet | Haughey, Maxwell B. Christensen, Kirsten E. Poole, Darren L. Donohoe, Timothy J. |
author_sort | Haughey, Maxwell B. |
collection | PubMed |
description | Through the use of model studies, an approach was conceived towards the synthesis of the taiwanschirin family of natural products. These are structurally complex compounds which represent highly challenging and biologically active targets for total synthesis. This work describes a successful synthesis of the complex taiwanschirin fused [8,6,5] core through a novel alkynylation reaction coupled with an intramolecular Heck reaction used to construct the 8-membered ring. |
format | Online Article Text |
id | pubmed-8528008 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-85280082021-11-12 Development of an enolate alkynylation approach towards the synthesis of the taiwanschirin natural products Haughey, Maxwell B. Christensen, Kirsten E. Poole, Darren L. Donohoe, Timothy J. Chem Sci Chemistry Through the use of model studies, an approach was conceived towards the synthesis of the taiwanschirin family of natural products. These are structurally complex compounds which represent highly challenging and biologically active targets for total synthesis. This work describes a successful synthesis of the complex taiwanschirin fused [8,6,5] core through a novel alkynylation reaction coupled with an intramolecular Heck reaction used to construct the 8-membered ring. The Royal Society of Chemistry 2021-09-20 /pmc/articles/PMC8528008/ /pubmed/34777757 http://dx.doi.org/10.1039/d1sc04247e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Haughey, Maxwell B. Christensen, Kirsten E. Poole, Darren L. Donohoe, Timothy J. Development of an enolate alkynylation approach towards the synthesis of the taiwanschirin natural products |
title | Development of an enolate alkynylation approach towards the synthesis of the taiwanschirin natural products |
title_full | Development of an enolate alkynylation approach towards the synthesis of the taiwanschirin natural products |
title_fullStr | Development of an enolate alkynylation approach towards the synthesis of the taiwanschirin natural products |
title_full_unstemmed | Development of an enolate alkynylation approach towards the synthesis of the taiwanschirin natural products |
title_short | Development of an enolate alkynylation approach towards the synthesis of the taiwanschirin natural products |
title_sort | development of an enolate alkynylation approach towards the synthesis of the taiwanschirin natural products |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8528008/ https://www.ncbi.nlm.nih.gov/pubmed/34777757 http://dx.doi.org/10.1039/d1sc04247e |
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