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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...

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Detalles Bibliográficos
Autores principales: Haughey, Maxwell B., Christensen, Kirsten E., Poole, Darren L., Donohoe, Timothy J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
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.
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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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