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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...

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Detalles Bibliográficos
Autores principales: Kobayashi, Kenichi, Kunimura, Risako, Kogen, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
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.
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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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