Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/66621
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dc.contributor.authorSingh, Samta-
dc.contributor.authorTiwari, Avinash-
dc.date.accessioned2025-10-22T08:37:52Z-
dc.date.available2025-10-22T08:37:52Z-
dc.date.issued2025-10-
dc.identifier.issn2583-1321 (Online); 0019-5103 (Print)-
dc.identifier.urihttp://nopr.niscpr.res.in/handle/123456789/66621-
dc.description995-997en_US
dc.description.abstractOne of the important and known processes in the chemistry of carbohydrates is the glycosylation reaction, in which C–O bonds are commonly used to join two different units. One of the most difficult but crucial aspects of glycochemistry to be addressed in the quest to advance this field is the design and development of sustainable catalytic methods for O-glycosylation. Herein, is described a straight forward and effective O-glycosylation technique using palladium as a catalyst, which involves triggering the activity of a phenylpropiolate glycoside donor.en_US
dc.language.isoenen_US
dc.publisherNIScPR - CSIRen_US
dc.sourceIJC Vol.64(10) [October 2025]en_US
dc.subjectPalladiumen_US
dc.subjectGlycosylationen_US
dc.subjectDonoren_US
dc.subjectIntermolecularen_US
dc.subjectNucleophilic additionen_US
dc.titleSynthesis of 6-isopropoxy-2-phenyl-4,4a,6,8atetrahydropyrano[ 3,2-d][1,3]dioxine via palladium catalysed O-glycosylationen_US
dc.identifier.doihttps://doi.org/10.56042/ijc.v64i10.13563en_US
Appears in Collections:IJC Vol.64(10) [October 2025]

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