Cargando…
First Total Synthesis of Varioxiranol A
The paper describes the first total synthesis of natural varioxiranol A by chiral pool approach and confirmation of its absolute configuration by single-crystal X-ray analysis. The target varioxiranol A and its 4-epimer were obtained after 10 steps from single and available chiral source 1,2-O-isopr...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6429112/ https://www.ncbi.nlm.nih.gov/pubmed/30823483 http://dx.doi.org/10.3390/molecules24050862 |
_version_ | 1783405521948114944 |
---|---|
author | Lásiková, Angelika Doháňošová, Jana Štiblariková, Mária Parák, Martin Moncol, Ján Gracza, Tibor |
author_facet | Lásiková, Angelika Doháňošová, Jana Štiblariková, Mária Parák, Martin Moncol, Ján Gracza, Tibor |
author_sort | Lásiková, Angelika |
collection | PubMed |
description | The paper describes the first total synthesis of natural varioxiranol A by chiral pool approach and confirmation of its absolute configuration by single-crystal X-ray analysis. The target varioxiranol A and its 4-epimer were obtained after 10 steps from single and available chiral source 1,2-O-isopropylidene-d-glyceraldehyde in an overall yield of 10% and 6%, respectively. A synthetic strategy based on the Julia–Kocieński coupling reaction between aromatic sulfone and corresponding aldose derivative makes it possible to prepare other interesting polyketide derivatives (varioxiranols B-G, varioxirane, varioxiranediols). |
format | Online Article Text |
id | pubmed-6429112 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-64291122019-04-15 First Total Synthesis of Varioxiranol A Lásiková, Angelika Doháňošová, Jana Štiblariková, Mária Parák, Martin Moncol, Ján Gracza, Tibor Molecules Article The paper describes the first total synthesis of natural varioxiranol A by chiral pool approach and confirmation of its absolute configuration by single-crystal X-ray analysis. The target varioxiranol A and its 4-epimer were obtained after 10 steps from single and available chiral source 1,2-O-isopropylidene-d-glyceraldehyde in an overall yield of 10% and 6%, respectively. A synthetic strategy based on the Julia–Kocieński coupling reaction between aromatic sulfone and corresponding aldose derivative makes it possible to prepare other interesting polyketide derivatives (varioxiranols B-G, varioxirane, varioxiranediols). MDPI 2019-02-28 /pmc/articles/PMC6429112/ /pubmed/30823483 http://dx.doi.org/10.3390/molecules24050862 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Lásiková, Angelika Doháňošová, Jana Štiblariková, Mária Parák, Martin Moncol, Ján Gracza, Tibor First Total Synthesis of Varioxiranol A |
title | First Total Synthesis of Varioxiranol A |
title_full | First Total Synthesis of Varioxiranol A |
title_fullStr | First Total Synthesis of Varioxiranol A |
title_full_unstemmed | First Total Synthesis of Varioxiranol A |
title_short | First Total Synthesis of Varioxiranol A |
title_sort | first total synthesis of varioxiranol a |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6429112/ https://www.ncbi.nlm.nih.gov/pubmed/30823483 http://dx.doi.org/10.3390/molecules24050862 |
work_keys_str_mv | AT lasikovaangelika firsttotalsynthesisofvarioxiranola AT dohanosovajana firsttotalsynthesisofvarioxiranola AT stiblarikovamaria firsttotalsynthesisofvarioxiranola AT parakmartin firsttotalsynthesisofvarioxiranola AT moncoljan firsttotalsynthesisofvarioxiranola AT graczatibor firsttotalsynthesisofvarioxiranola |