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Partial Synthesis of Crassicauline A from Yunaconitine

ABSTRACT: Both Aconitum hemsleyanum and Aconitum geniculatun have abundant contents of yunaconitine (1). Yunaconitine (1) has similar skeleton to crassicauline A (3); the only difference between them is that 1 contains a α-hydroxyl group at C-3. Our team attempts to convert 1 into 3 because 3 owns p...

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Autores principales: Zhang, Rong-Ping, Lin, Yan-Jun, Yu, Hao-Fei, Chen, Si-Ying, Zhou, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Singapore 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7176785/
https://www.ncbi.nlm.nih.gov/pubmed/32297141
http://dx.doi.org/10.1007/s13659-020-00238-0
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author Zhang, Rong-Ping
Lin, Yan-Jun
Yu, Hao-Fei
Chen, Si-Ying
Zhou, Jun
author_facet Zhang, Rong-Ping
Lin, Yan-Jun
Yu, Hao-Fei
Chen, Si-Ying
Zhou, Jun
author_sort Zhang, Rong-Ping
collection PubMed
description ABSTRACT: Both Aconitum hemsleyanum and Aconitum geniculatun have abundant contents of yunaconitine (1). Yunaconitine (1) has similar skeleton to crassicauline A (3); the only difference between them is that 1 contains a α-hydroxyl group at C-3. Our team attempts to convert 1 into 3 because 3 owns pharmacological activity. There are two steps to achieve the transformation above: firstly, use dehydration reaction to transform yunaconitine (1) into dehydroyunaconitine (2); secondly, use hydrogen reduction to acquire crassicauline A (3). Compared with other methods, this one below is more suitable for production application and more concise; moreover, the cost is lower with higher yield. GRAPHIC ABSTRACT: [Image: see text]
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spelling pubmed-71767852020-04-28 Partial Synthesis of Crassicauline A from Yunaconitine Zhang, Rong-Ping Lin, Yan-Jun Yu, Hao-Fei Chen, Si-Ying Zhou, Jun Nat Prod Bioprospect Original Article ABSTRACT: Both Aconitum hemsleyanum and Aconitum geniculatun have abundant contents of yunaconitine (1). Yunaconitine (1) has similar skeleton to crassicauline A (3); the only difference between them is that 1 contains a α-hydroxyl group at C-3. Our team attempts to convert 1 into 3 because 3 owns pharmacological activity. There are two steps to achieve the transformation above: firstly, use dehydration reaction to transform yunaconitine (1) into dehydroyunaconitine (2); secondly, use hydrogen reduction to acquire crassicauline A (3). Compared with other methods, this one below is more suitable for production application and more concise; moreover, the cost is lower with higher yield. GRAPHIC ABSTRACT: [Image: see text] Springer Singapore 2020-04-15 /pmc/articles/PMC7176785/ /pubmed/32297141 http://dx.doi.org/10.1007/s13659-020-00238-0 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Original Article
Zhang, Rong-Ping
Lin, Yan-Jun
Yu, Hao-Fei
Chen, Si-Ying
Zhou, Jun
Partial Synthesis of Crassicauline A from Yunaconitine
title Partial Synthesis of Crassicauline A from Yunaconitine
title_full Partial Synthesis of Crassicauline A from Yunaconitine
title_fullStr Partial Synthesis of Crassicauline A from Yunaconitine
title_full_unstemmed Partial Synthesis of Crassicauline A from Yunaconitine
title_short Partial Synthesis of Crassicauline A from Yunaconitine
title_sort partial synthesis of crassicauline a from yunaconitine
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7176785/
https://www.ncbi.nlm.nih.gov/pubmed/32297141
http://dx.doi.org/10.1007/s13659-020-00238-0
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