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dc.contributor.authorVysabhattar, Ramanen_US
dc.contributor.authorGANESH, KRISHNA N.en_US
dc.date.accessioned2019-01-21T10:29:25Z
dc.date.available2019-01-21T10:29:25Z
dc.date.issued2010-12en_US
dc.identifier.citationTetrahedron Letters, Vol. 50(51).en_US
dc.identifier.issn0040-4039en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1489-
dc.identifier.urihttps://doi.org/10.1016/j.tetlet.2010.10.040en_US
dc.description.abstractA new, novel and efficient in situ synthesis of 8-aminoadeninyl PNA oligomers from corresponding 8-bromoadeninyl PNA oligomers is reported. The study of hybridisation properties of (8-Br/8-NH2) PNA oligomers with cDNA reveals substitution-site dependent stabilization of derived triplexes and duplexes.en_US
dc.language.isoenen_US
dc.publisherElsevier B.V.en_US
dc.subjectPeptide nucleic aciden_US
dc.subjectMedicinal chemistryen_US
dc.subjectDNA and RNAen_US
dc.subjectPyrimidine PNA sequenceen_US
dc.subjectTrifluoromethane sulphonic aciden_US
dc.subject2010en_US
dc.titleIn situ, on-resin synthesis of 8-Br/NH2 adeninyl peptide nucleic acid (PNA) oligomers and complementation studies with DNAen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleTetrahedron Lettersen_US
dc.publication.originofpublisherForeignen_US
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