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Hyperacmosins K–M, three new polycyclic polyprenylated acylphloroglucinols from Hypericum acmosepalum

Hyperacmosins K–M (1–3), three new polycyclic polyprenylated acylphloroglucinol (PPAPs) derivatives, were isolated from the air-dried aerial parts of Hypericum asmosepalum. Compounds 1 and 2 both possessed a rare 5,5-spiroketal subunit with the loss of C-2′ carbonyl in the phloroglucinal ring, while...

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Autores principales: Sun, Mingxia, Wang, Xue, Zhu, Tingting, Suo, Xinyue, Wang, Jiajia, Ji, Tengfei, Liu, Bo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9034054/
https://www.ncbi.nlm.nih.gov/pubmed/35479371
http://dx.doi.org/10.1039/d1ra03533a
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author Sun, Mingxia
Wang, Xue
Zhu, Tingting
Suo, Xinyue
Wang, Jiajia
Ji, Tengfei
Liu, Bo
author_facet Sun, Mingxia
Wang, Xue
Zhu, Tingting
Suo, Xinyue
Wang, Jiajia
Ji, Tengfei
Liu, Bo
author_sort Sun, Mingxia
collection PubMed
description Hyperacmosins K–M (1–3), three new polycyclic polyprenylated acylphloroglucinol (PPAPs) derivatives, were isolated from the air-dried aerial parts of Hypericum asmosepalum. Compounds 1 and 2 both possessed a rare 5,5-spiroketal subunit with the loss of C-2′ carbonyl in the phloroglucinal ring, while compound 3 featured an unusual 1,2-seco-bicyclo[3.3.1] PPAP skeleton. Their structures were confirmed by NMR, HRESIMS, and CD spectra. The plausible biogenetic pathways of 1–3 were proposed, which gave an insight for future biomimetic synthesis of the novel compounds.
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spelling pubmed-90340542022-04-26 Hyperacmosins K–M, three new polycyclic polyprenylated acylphloroglucinols from Hypericum acmosepalum Sun, Mingxia Wang, Xue Zhu, Tingting Suo, Xinyue Wang, Jiajia Ji, Tengfei Liu, Bo RSC Adv Chemistry Hyperacmosins K–M (1–3), three new polycyclic polyprenylated acylphloroglucinol (PPAPs) derivatives, were isolated from the air-dried aerial parts of Hypericum asmosepalum. Compounds 1 and 2 both possessed a rare 5,5-spiroketal subunit with the loss of C-2′ carbonyl in the phloroglucinal ring, while compound 3 featured an unusual 1,2-seco-bicyclo[3.3.1] PPAP skeleton. Their structures were confirmed by NMR, HRESIMS, and CD spectra. The plausible biogenetic pathways of 1–3 were proposed, which gave an insight for future biomimetic synthesis of the novel compounds. The Royal Society of Chemistry 2021-06-14 /pmc/articles/PMC9034054/ /pubmed/35479371 http://dx.doi.org/10.1039/d1ra03533a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Sun, Mingxia
Wang, Xue
Zhu, Tingting
Suo, Xinyue
Wang, Jiajia
Ji, Tengfei
Liu, Bo
Hyperacmosins K–M, three new polycyclic polyprenylated acylphloroglucinols from Hypericum acmosepalum
title Hyperacmosins K–M, three new polycyclic polyprenylated acylphloroglucinols from Hypericum acmosepalum
title_full Hyperacmosins K–M, three new polycyclic polyprenylated acylphloroglucinols from Hypericum acmosepalum
title_fullStr Hyperacmosins K–M, three new polycyclic polyprenylated acylphloroglucinols from Hypericum acmosepalum
title_full_unstemmed Hyperacmosins K–M, three new polycyclic polyprenylated acylphloroglucinols from Hypericum acmosepalum
title_short Hyperacmosins K–M, three new polycyclic polyprenylated acylphloroglucinols from Hypericum acmosepalum
title_sort hyperacmosins k–m, three new polycyclic polyprenylated acylphloroglucinols from hypericum acmosepalum
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9034054/
https://www.ncbi.nlm.nih.gov/pubmed/35479371
http://dx.doi.org/10.1039/d1ra03533a
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