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Concise Enantiospecific Total Synthesis of Tubingensin A
[Image: see text] We report the enantiospecific total synthesis of (+)-tubingensin A. Our synthesis features an aryne cyclization to efficiently introduce the vicinal quaternary stereocenters of the natural product and proceeds in only nine steps (longest linear sequence) from known compounds.
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3985696/ https://www.ncbi.nlm.nih.gov/pubmed/24524351 http://dx.doi.org/10.1021/ja501142e |
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author | Goetz, Adam E. Silberstein, Amanda L. Corsello, Michael A. Garg, Neil K. |
author_facet | Goetz, Adam E. Silberstein, Amanda L. Corsello, Michael A. Garg, Neil K. |
author_sort | Goetz, Adam E. |
collection | PubMed |
description | [Image: see text] We report the enantiospecific total synthesis of (+)-tubingensin A. Our synthesis features an aryne cyclization to efficiently introduce the vicinal quaternary stereocenters of the natural product and proceeds in only nine steps (longest linear sequence) from known compounds. |
format | Online Article Text |
id | pubmed-3985696 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-39856962015-02-14 Concise Enantiospecific Total Synthesis of Tubingensin A Goetz, Adam E. Silberstein, Amanda L. Corsello, Michael A. Garg, Neil K. J Am Chem Soc [Image: see text] We report the enantiospecific total synthesis of (+)-tubingensin A. Our synthesis features an aryne cyclization to efficiently introduce the vicinal quaternary stereocenters of the natural product and proceeds in only nine steps (longest linear sequence) from known compounds. American Chemical Society 2014-02-14 2014-02-26 /pmc/articles/PMC3985696/ /pubmed/24524351 http://dx.doi.org/10.1021/ja501142e Text en Copyright © 2014 American Chemical Society |
spellingShingle | Goetz, Adam E. Silberstein, Amanda L. Corsello, Michael A. Garg, Neil K. Concise Enantiospecific Total Synthesis of Tubingensin A |
title | Concise
Enantiospecific Total Synthesis of Tubingensin
A |
title_full | Concise
Enantiospecific Total Synthesis of Tubingensin
A |
title_fullStr | Concise
Enantiospecific Total Synthesis of Tubingensin
A |
title_full_unstemmed | Concise
Enantiospecific Total Synthesis of Tubingensin
A |
title_short | Concise
Enantiospecific Total Synthesis of Tubingensin
A |
title_sort | concise
enantiospecific total synthesis of tubingensin
a |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3985696/ https://www.ncbi.nlm.nih.gov/pubmed/24524351 http://dx.doi.org/10.1021/ja501142e |
work_keys_str_mv | AT goetzadame conciseenantiospecifictotalsynthesisoftubingensina AT silbersteinamandal conciseenantiospecifictotalsynthesisoftubingensina AT corsellomichaela conciseenantiospecifictotalsynthesisoftubingensina AT gargneilk conciseenantiospecifictotalsynthesisoftubingensina |