| ID | 63881 |
| FullText URL | |
| Author |
Abe, Takumi
Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
ORCID
Kaken ID
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Nakajima, Ren
Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
Yamashiro, Toshiki
Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
Sawada, Daisuke
Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
Kaken ID
researchmap
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| Abstract | Echinosulfonic acid D, a sponge metabolite whose structure was recently reassigned, was synthesized for the first time. The key step is the double indolization of dimethylbarbituric acid using the umpolung indole reagent, followed by a hydrolysis/decarboxylation/esterification sequence.
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| Note | This document is the Accepted Manuscript version of a Published Work that appeared in final form in [Journal of Natural Products], copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acs.jnatprod.2c00559
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| Published Date | 2022-08-17
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| Publication Title |
Journal of Natural Products
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| Volume | volume85
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| Issue | issue8
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| Publisher | American Chemical Society (ACS)
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| Start Page | 2122
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| End Page | 2125
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| ISSN | 0163-3864
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| Content Type |
Journal Article
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| language |
English
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| OAI-PMH Set |
岡山大学
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| Copyright Holders | © 2022 American Chemical Society and American Society of Pharmacognosy
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| File Version | author
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| PubMed ID | |
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| Web of Science KeyUT | |
| Related Url | isVersionOf https://doi.org/10.1021/acs.jnatprod.2c00559
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| Funder Name |
Japan Society for the Promotion of Science
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| 助成番号 | 17H06173
22K06503
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