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Synthesis of acremines A, B and F and studies on the bisacremines
The acremines are a family of meroterpenoids isolated from fungi of the genus Acremonium. Here, we present the asymmetric total synthesis of acremine F which hinges on a modestly enantioselective dihydroxylation and a subsequent kinetic resolution via a highly selective asymmetric reduction. Chemose...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6774081/ https://www.ncbi.nlm.nih.gov/pubmed/31598179 http://dx.doi.org/10.3762/bjoc.15.219 |
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author | Winter, Nils Trauner, Dirk |
author_facet | Winter, Nils Trauner, Dirk |
author_sort | Winter, Nils |
collection | PubMed |
description | The acremines are a family of meroterpenoids isolated from fungi of the genus Acremonium. Here, we present the asymmetric total synthesis of acremine F which hinges on a modestly enantioselective dihydroxylation and a subsequent kinetic resolution via a highly selective asymmetric reduction. Chemoselective oxidation of acremine F gave access to acremines A and B. The dimerization of acremine F to bisacremine E was investigated but could not be achieved, shedding light on the formation of the acremine dimers in nature. |
format | Online Article Text |
id | pubmed-6774081 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-67740812019-10-09 Synthesis of acremines A, B and F and studies on the bisacremines Winter, Nils Trauner, Dirk Beilstein J Org Chem Full Research Paper The acremines are a family of meroterpenoids isolated from fungi of the genus Acremonium. Here, we present the asymmetric total synthesis of acremine F which hinges on a modestly enantioselective dihydroxylation and a subsequent kinetic resolution via a highly selective asymmetric reduction. Chemoselective oxidation of acremine F gave access to acremines A and B. The dimerization of acremine F to bisacremine E was investigated but could not be achieved, shedding light on the formation of the acremine dimers in nature. Beilstein-Institut 2019-09-23 /pmc/articles/PMC6774081/ /pubmed/31598179 http://dx.doi.org/10.3762/bjoc.15.219 Text en Copyright © 2019, Winter and Trauner https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0). Please note that the reuse, redistribution and reproduction in particular requires that the authors and source are credited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Full Research Paper Winter, Nils Trauner, Dirk Synthesis of acremines A, B and F and studies on the bisacremines |
title | Synthesis of acremines A, B and F and studies on the bisacremines |
title_full | Synthesis of acremines A, B and F and studies on the bisacremines |
title_fullStr | Synthesis of acremines A, B and F and studies on the bisacremines |
title_full_unstemmed | Synthesis of acremines A, B and F and studies on the bisacremines |
title_short | Synthesis of acremines A, B and F and studies on the bisacremines |
title_sort | synthesis of acremines a, b and f and studies on the bisacremines |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6774081/ https://www.ncbi.nlm.nih.gov/pubmed/31598179 http://dx.doi.org/10.3762/bjoc.15.219 |
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