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Synthesis of Anemoclemosides A and B, Two Saponins Isolated from Anemoclema glaucifolium
Bangor Univ, Sch Chem, Deiniol Rd, Bangor LL57 2UW, Gwynedd, Wales..ORCID iD: 0000-0002-5820-6314
Bangor Univ, Sch Chem, Deiniol Rd, Bangor LL57 2UW, Gwynedd, Wales..
Bangor Univ, Sch Chem, Deiniol Rd, Bangor LL57 2UW, Gwynedd, Wales..
Bangor Univ, Sch Chem, Deiniol Rd, Bangor LL57 2UW, Gwynedd, Wales..
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2020 (English)In: European Journal of Organic Chemistry, ISSN 1434-193X, E-ISSN 1099-0690, Vol. 2020, no 48, p. 7470-7473Article in journal (Refereed) Published
Abstract [en]

Steroidal and triterpenoid saponins are attractive for their wide-ranging pharmacological properties. The triterpenoid saponins Anemoclemoside A and B are root constituents of the Chinese folk medicinal plant Anemoclema glaucifolium (Ranunculaceae). Both compounds feature an unusual cyclic acetal linkage to the carbohydrate l-arabinose in its open chain form rather than the typical glycosidic bond present in normal saponins. The straightforward and scalable syntheses of both saponins starting from l-arabinose as well as l-lyxose and l-rhamnose are described.

Place, publisher, year, edition, pages
Wiley , 2020. Vol. 2020, no 48, p. 7470-7473
Keywords [en]
Saponins, Anemoclemosides, Glycosylation, Hederagenin glycosides, Cyclic acetal glycosidic linkage
National Category
Organic Chemistry
Identifiers
URN: urn:nbn:se:kth:diva-305689DOI: 10.1002/ejoc.202001317ISI: 000588113200001Scopus ID: 2-s2.0-85096646416OAI: oai:DiVA.org:kth-305689DiVA, id: diva2:1617269
Note

QC 20211206

Available from: 2021-12-06 Created: 2021-12-06 Last updated: 2022-06-25Bibliographically approved

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Lahmann, Martina

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Bouillon, Marc E.Lahmann, Martina
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