Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1595
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dc.contributor.authorRao, Boddu Venkateswaraen_US
dc.contributor.authorDhokale, Snehalen_US
dc.contributor.authorRajamohanan, Pattuparambil R.en_US
dc.contributor.authorHOTHA, SRINIVASen_US
dc.date.accessioned2019-02-14T05:00:09Z
dc.date.available2019-02-14T05:00:09Z
dc.date.issued2013-09en_US
dc.identifier.citationChemical Communications, 49(92), 10808-10810.en_US
dc.identifier.issn1359-7345en_US
dc.identifier.issn1364-548Xen_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1595-
dc.identifier.urihttps://doi.org/10.1039/C3CC46634Een_US
dc.description.abstractConjugation is an important reaction that enables coupling of molecules. Many protocols exist for the synthesis of binary conjugates from two different molecules or for the polyvalent display of a single molecule. There aren't many methods for the synthesis of ternary conjugates. However, methods for ternary conjugation are important for understanding the interplay of interactions between three biomolecules (or any three molecules per se). A strategy for ternary bioconjugation using inverse electron demand Diels-Alder reaction with tetrazine is studied. Ternary conjugation was demonstrated by the reaction of a model glyco-peptide binary conjugate with a fluorescent tagged olefin.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectTetrazine templateden_US
dc.subjectSynthesis of ternaryen_US
dc.subjectCoupling of moleculesen_US
dc.subjectFluorescent tagged olefinen_US
dc.subject2013en_US
dc.titleA tetrazine templated method for the synthesis of ternary conjugatesen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleChemical Communicationsen_US
dc.publication.originofpublisherForeignen_US
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