Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/4959
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dc.contributor.authorManiyamma, A-
dc.contributor.authorSadik N, M-
dc.contributor.authorPurushothaman C., H-
dc.contributor.authorSasikumar, P-
dc.contributor.authorRadhakrishnan, K V-
dc.contributor.authorRavi S, L-
dc.date.accessioned2025-07-12T09:26:12Z-
dc.date.available2025-07-12T09:26:12Z-
dc.date.issued2024-01-
dc.identifier.citationOrganic & Biomolecular Chemistry; 22(1):65-69en_US
dc.identifier.urihttps://pubs.rsc.org/en/content/articlelanding/2024/ob/d3ob01633a-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/4959-
dc.description.abstractA method involving stereoselective glycosylation catalyzed by (+)-isomenthol ester of pentacarbomethoxycyclopentadiene as a chiral Brønsted acid, with n-pentenyl glycosides in the presence of N-iodosuccinimide as the promoter is described; this method offered a chiral recognition of racemic substrates.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.titleα/β-Stereo- and diastereoselective glycosylation with n-pentenyl glycoside donors, promoted by N-iodosuccinimide and catalyzed by chiral Brønsted aciden_US
dc.typeArticleen_US
Appears in Collections:2024



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