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Total Synthesis of Parameritannin A2, a Branched Epicatechin Tetramer with Two Double Linkages

The first total synthesis of parameritannin A2 (1), a branched epicatechin (EC) tetramer is reported. The “phloroglucinol trick” was used to circumvent two synthetic issues encountered when assembling four EC units, namely, the steric constraint and the formation of the C4−C6 interflavan linkage. As...

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Detalles Bibliográficos
Autores principales: Betkekar, Vipul V., Suzuki, Keisuke, Ohmori, Ken
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9401032/
https://www.ncbi.nlm.nih.gov/pubmed/35534438
http://dx.doi.org/10.1002/anie.202205106
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author Betkekar, Vipul V.
Suzuki, Keisuke
Ohmori, Ken
author_facet Betkekar, Vipul V.
Suzuki, Keisuke
Ohmori, Ken
author_sort Betkekar, Vipul V.
collection PubMed
description The first total synthesis of parameritannin A2 (1), a branched epicatechin (EC) tetramer is reported. The “phloroglucinol trick” was used to circumvent two synthetic issues encountered when assembling four EC units, namely, the steric constraint and the formation of the C4−C6 interflavan linkage. As a substructure of the middle EC unit, phloroglucinol enabled the single‐step assembly of two EC units (top and side) through A‐type linkages. The middle EC unit was constructed by conducting a newly developed three‐carbon flavan annulation via a Pummerer/Friedel–Crafts cascade reaction to furnish a trimeric intermediate bearing a thio‐leaving group at C4 position, which allowed the final installation of the bottom EC unit.
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spelling pubmed-94010322022-08-26 Total Synthesis of Parameritannin A2, a Branched Epicatechin Tetramer with Two Double Linkages Betkekar, Vipul V. Suzuki, Keisuke Ohmori, Ken Angew Chem Int Ed Engl Research Articles The first total synthesis of parameritannin A2 (1), a branched epicatechin (EC) tetramer is reported. The “phloroglucinol trick” was used to circumvent two synthetic issues encountered when assembling four EC units, namely, the steric constraint and the formation of the C4−C6 interflavan linkage. As a substructure of the middle EC unit, phloroglucinol enabled the single‐step assembly of two EC units (top and side) through A‐type linkages. The middle EC unit was constructed by conducting a newly developed three‐carbon flavan annulation via a Pummerer/Friedel–Crafts cascade reaction to furnish a trimeric intermediate bearing a thio‐leaving group at C4 position, which allowed the final installation of the bottom EC unit. John Wiley and Sons Inc. 2022-05-20 2022-07-11 /pmc/articles/PMC9401032/ /pubmed/35534438 http://dx.doi.org/10.1002/anie.202205106 Text en © 2022 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Betkekar, Vipul V.
Suzuki, Keisuke
Ohmori, Ken
Total Synthesis of Parameritannin A2, a Branched Epicatechin Tetramer with Two Double Linkages
title Total Synthesis of Parameritannin A2, a Branched Epicatechin Tetramer with Two Double Linkages
title_full Total Synthesis of Parameritannin A2, a Branched Epicatechin Tetramer with Two Double Linkages
title_fullStr Total Synthesis of Parameritannin A2, a Branched Epicatechin Tetramer with Two Double Linkages
title_full_unstemmed Total Synthesis of Parameritannin A2, a Branched Epicatechin Tetramer with Two Double Linkages
title_short Total Synthesis of Parameritannin A2, a Branched Epicatechin Tetramer with Two Double Linkages
title_sort total synthesis of parameritannin a2, a branched epicatechin tetramer with two double linkages
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9401032/
https://www.ncbi.nlm.nih.gov/pubmed/35534438
http://dx.doi.org/10.1002/anie.202205106
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