Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Winter, Nils, Trauner, Dirk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2019
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
_version_ 1783456034729230336
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
work_keys_str_mv AT winternils synthesisofacreminesabandfandstudiesonthebisacremines
AT traunerdirk synthesisofacreminesabandfandstudiesonthebisacremines