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Synthesis of Oxazocenones via Gold(I)-Catalyzed 8-Endo-Dig Hydroalkoxylation of Alkynamides
[Image: see text] Several benzoxazocenones have been found to exhibit novel cellular activities. In the present study, we report a gold(I)-catalyzed 8-endo-dig hydroalkoxylation reaction of alkynamides to access analogous oxazocenone scaffolds. This methodology provided an advanced intermediate, whi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4323038/ https://www.ncbi.nlm.nih.gov/pubmed/25569027 http://dx.doi.org/10.1021/ol503273v |
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author | Scully, Stephen S. Zheng, Shao-Liang Wagner, Bridget K. Schreiber, Stuart L. |
author_facet | Scully, Stephen S. Zheng, Shao-Liang Wagner, Bridget K. Schreiber, Stuart L. |
author_sort | Scully, Stephen S. |
collection | PubMed |
description | [Image: see text] Several benzoxazocenones have been found to exhibit novel cellular activities. In the present study, we report a gold(I)-catalyzed 8-endo-dig hydroalkoxylation reaction of alkynamides to access analogous oxazocenone scaffolds. This methodology provided an advanced intermediate, which was elaborated to a des-benzo analog of a bioactive benzoxazocenone. |
format | Online Article Text |
id | pubmed-4323038 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-43230382016-01-08 Synthesis of Oxazocenones via Gold(I)-Catalyzed 8-Endo-Dig Hydroalkoxylation of Alkynamides Scully, Stephen S. Zheng, Shao-Liang Wagner, Bridget K. Schreiber, Stuart L. Org Lett [Image: see text] Several benzoxazocenones have been found to exhibit novel cellular activities. In the present study, we report a gold(I)-catalyzed 8-endo-dig hydroalkoxylation reaction of alkynamides to access analogous oxazocenone scaffolds. This methodology provided an advanced intermediate, which was elaborated to a des-benzo analog of a bioactive benzoxazocenone. American Chemical Society 2015-01-08 2015-02-06 /pmc/articles/PMC4323038/ /pubmed/25569027 http://dx.doi.org/10.1021/ol503273v Text en Copyright © 2015 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Scully, Stephen S. Zheng, Shao-Liang Wagner, Bridget K. Schreiber, Stuart L. Synthesis of Oxazocenones via Gold(I)-Catalyzed 8-Endo-Dig Hydroalkoxylation of Alkynamides |
title | Synthesis of Oxazocenones via Gold(I)-Catalyzed 8-Endo-Dig Hydroalkoxylation of Alkynamides |
title_full | Synthesis of Oxazocenones via Gold(I)-Catalyzed 8-Endo-Dig Hydroalkoxylation of Alkynamides |
title_fullStr | Synthesis of Oxazocenones via Gold(I)-Catalyzed 8-Endo-Dig Hydroalkoxylation of Alkynamides |
title_full_unstemmed | Synthesis of Oxazocenones via Gold(I)-Catalyzed 8-Endo-Dig Hydroalkoxylation of Alkynamides |
title_short | Synthesis of Oxazocenones via Gold(I)-Catalyzed 8-Endo-Dig Hydroalkoxylation of Alkynamides |
title_sort | synthesis of oxazocenones via gold(i)-catalyzed 8-endo-dig hydroalkoxylation of alkynamides |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4323038/ https://www.ncbi.nlm.nih.gov/pubmed/25569027 http://dx.doi.org/10.1021/ol503273v |
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