Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/60726
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dc.contributor.authorAnnapurna, K-
dc.contributor.authorRao, K Srinivasa-
dc.contributor.authorNarsaiah, A Venkat-
dc.date.accessioned2022-10-21T06:00:07Z-
dc.date.available2022-10-21T06:00:07Z-
dc.date.issued2022-10-
dc.identifier.issn2583-1321 (Online); 0019-5103 (Print)-
dc.identifier.urihttp://nopr.niscpr.res.in/handle/123456789/60726-
dc.description1039-1045en_US
dc.description.abstractSynthesis of naturally occurring Sinuxylamides A-E has been accomplished. Synthesis started from commercially available L-tyrosine. The key reactions involved in this synthesis are amide formation, Mitsunobu etherification and ester hydrolysis.en_US
dc.language.isoenen_US
dc.publisherNIScPR-CSIR,Indiaen_US
dc.sourceIJC Vol.61(10) [Oct 2022]en_US
dc.subjectL-Tyrosineen_US
dc.subjectAmideen_US
dc.subjectEtherificationen_US
dc.subjectGlycoproteinen_US
dc.subjectMarine productsen_US
dc.titleSynthesis of glycoprotein inhibitory agents sinuxylamide A-Een_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.56042/ijc.v61i10.64005en_US
Appears in Collections:IJC Vol.61(10) [Oct 2022]

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