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11-Step Total Synthesis of Araiosamines
[Image: see text] A concise route to a small family of exotic marine alkaloids known as the araiosamines has been developed, and their absolute configuration has been assigned. The dense array of functionality, high polarity, and rich stereochemistry coupled with equilibrating topologies present an...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5095662/ https://www.ncbi.nlm.nih.gov/pubmed/27748593 http://dx.doi.org/10.1021/jacs.6b09701 |
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author | Tian, Maoqun Yan, Ming Baran, Phil S. |
author_facet | Tian, Maoqun Yan, Ming Baran, Phil S. |
author_sort | Tian, Maoqun |
collection | PubMed |
description | [Image: see text] A concise route to a small family of exotic marine alkaloids known as the araiosamines has been developed, and their absolute configuration has been assigned. The dense array of functionality, high polarity, and rich stereochemistry coupled with equilibrating topologies present an unusual challenge for chemical synthesis and an opportunity for innovation. Key steps involve the use of a new reagent for guanidine installation, a remarkably selective C–H functionalization, and a surprisingly simple final step that intersects a presumed biosynthetic intermediate. Synthetic araiosamines were shown to exhibit potency against Gram-positive and -negative bacteria despite a contrary report of no activity. |
format | Online Article Text |
id | pubmed-5095662 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-50956622016-11-07 11-Step Total Synthesis of Araiosamines Tian, Maoqun Yan, Ming Baran, Phil S. J Am Chem Soc [Image: see text] A concise route to a small family of exotic marine alkaloids known as the araiosamines has been developed, and their absolute configuration has been assigned. The dense array of functionality, high polarity, and rich stereochemistry coupled with equilibrating topologies present an unusual challenge for chemical synthesis and an opportunity for innovation. Key steps involve the use of a new reagent for guanidine installation, a remarkably selective C–H functionalization, and a surprisingly simple final step that intersects a presumed biosynthetic intermediate. Synthetic araiosamines were shown to exhibit potency against Gram-positive and -negative bacteria despite a contrary report of no activity. American Chemical Society 2016-10-17 2016-11-02 /pmc/articles/PMC5095662/ /pubmed/27748593 http://dx.doi.org/10.1021/jacs.6b09701 Text en Copyright © 2016 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 | Tian, Maoqun Yan, Ming Baran, Phil S. 11-Step Total Synthesis of Araiosamines |
title | 11-Step
Total Synthesis of Araiosamines |
title_full | 11-Step
Total Synthesis of Araiosamines |
title_fullStr | 11-Step
Total Synthesis of Araiosamines |
title_full_unstemmed | 11-Step
Total Synthesis of Araiosamines |
title_short | 11-Step
Total Synthesis of Araiosamines |
title_sort | 11-step
total synthesis of araiosamines |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5095662/ https://www.ncbi.nlm.nih.gov/pubmed/27748593 http://dx.doi.org/10.1021/jacs.6b09701 |
work_keys_str_mv | AT tianmaoqun 11steptotalsynthesisofaraiosamines AT yanming 11steptotalsynthesisofaraiosamines AT baranphils 11steptotalsynthesisofaraiosamines |