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A tetrazine templated method for the synthesis of ternary conjugates

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dc.contributor.author Rao, Boddu Venkateswara en_US
dc.contributor.author Dhokale, Snehal en_US
dc.contributor.author Rajamohanan, Pattuparambil R. en_US
dc.contributor.author HOTHA, SRINIVAS en_US
dc.date.accessioned 2019-02-14T05:00:09Z
dc.date.available 2019-02-14T05:00:09Z
dc.date.issued 2013-09 en_US
dc.identifier.citation Chemical Communications, 49(92), 10808-10810. en_US
dc.identifier.issn 1359-7345 en_US
dc.identifier.issn 1364-548X en_US
dc.identifier.uri http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1595
dc.identifier.uri https://doi.org/10.1039/C3CC46634E en_US
dc.description.abstract Conjugation 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.iso en en_US
dc.publisher Royal Society of Chemistry en_US
dc.subject Tetrazine templated en_US
dc.subject Synthesis of ternary en_US
dc.subject Coupling of molecules en_US
dc.subject Fluorescent tagged olefin en_US
dc.subject 2013 en_US
dc.title A tetrazine templated method for the synthesis of ternary conjugates en_US
dc.type Article en_US
dc.contributor.department Dept. of Chemistry en_US
dc.identifier.sourcetitle Chemical Communications en_US
dc.publication.originofpublisher Foreign en_US


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