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Total Synthesis of the Proposed Structure of Paraphaeosphaeride C †
Paraphaeosphaeride C is a demethoxy derivative of phaeosphaeride A and exhibits STAT3 inhibitory activity. Our previous papers reported the total synthesis of phaeosphaeride A using a diastereoselective vinyl anion aldol reaction as the key step to construct the dihydropyran ring. In this work, the...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6930451/ https://www.ncbi.nlm.nih.gov/pubmed/31766322 http://dx.doi.org/10.3390/molecules24234230 |
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author | Kobayashi, Kenichi Kunimura, Risako Kogen, Hiroshi |
author_facet | Kobayashi, Kenichi Kunimura, Risako Kogen, Hiroshi |
author_sort | Kobayashi, Kenichi |
collection | PubMed |
description | Paraphaeosphaeride C is a demethoxy derivative of phaeosphaeride A and exhibits STAT3 inhibitory activity. Our previous papers reported the total synthesis of phaeosphaeride A using a diastereoselective vinyl anion aldol reaction as the key step to construct the dihydropyran ring. In this work, the first total synthesis of the proposed structure of paraphaeosphaeride C was achieved via a similar synthetic strategy. The synthetic compound was characterized through extensive nuclear magnetic resonance (NMR) analysis but the (1)H and (13)C-NMR data for this compound did not correspond to those reported in the literature for paraphaeosphaeride C. |
format | Online Article Text |
id | pubmed-6930451 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-69304512019-12-26 Total Synthesis of the Proposed Structure of Paraphaeosphaeride C † Kobayashi, Kenichi Kunimura, Risako Kogen, Hiroshi Molecules Communication Paraphaeosphaeride C is a demethoxy derivative of phaeosphaeride A and exhibits STAT3 inhibitory activity. Our previous papers reported the total synthesis of phaeosphaeride A using a diastereoselective vinyl anion aldol reaction as the key step to construct the dihydropyran ring. In this work, the first total synthesis of the proposed structure of paraphaeosphaeride C was achieved via a similar synthetic strategy. The synthetic compound was characterized through extensive nuclear magnetic resonance (NMR) analysis but the (1)H and (13)C-NMR data for this compound did not correspond to those reported in the literature for paraphaeosphaeride C. MDPI 2019-11-21 /pmc/articles/PMC6930451/ /pubmed/31766322 http://dx.doi.org/10.3390/molecules24234230 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 | Communication Kobayashi, Kenichi Kunimura, Risako Kogen, Hiroshi Total Synthesis of the Proposed Structure of Paraphaeosphaeride C † |
title | Total Synthesis of the Proposed Structure of Paraphaeosphaeride C † |
title_full | Total Synthesis of the Proposed Structure of Paraphaeosphaeride C † |
title_fullStr | Total Synthesis of the Proposed Structure of Paraphaeosphaeride C † |
title_full_unstemmed | Total Synthesis of the Proposed Structure of Paraphaeosphaeride C † |
title_short | Total Synthesis of the Proposed Structure of Paraphaeosphaeride C † |
title_sort | total synthesis of the proposed structure of paraphaeosphaeride c † |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6930451/ https://www.ncbi.nlm.nih.gov/pubmed/31766322 http://dx.doi.org/10.3390/molecules24234230 |
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