Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Tian, Maoqun, Yan, Ming, Baran, Phil S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2016
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
_version_ 1782465325107773440
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