Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/7542
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dc.contributor.authorSHIRAJ, ABDULen_US
dc.contributor.authorRamabhadran, Raghunath O.en_US
dc.contributor.authorGANESH, KRISHNA N.en_US
dc.date.accessioned2022-12-28T09:21:55Z-
dc.date.available2022-12-28T09:21:55Z-
dc.date.issued2022-10en_US
dc.identifier.citationOrganic Letters, 24(40), 7421–7427.en_US
dc.identifier.issn1523-7060en_US
dc.identifier.issn1523-7052en_US
dc.identifier.urihttps://doi.org/10.1021/acs.orglett.2c02993en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/7542-
dc.description.abstractThe replacement of α(CH2) by NH in monomers of standard aeg PNA and its homologue β-ala PNA leads to respective aza-PNA monomers (1 and 2) in which the NαH can form either an 8-membered H-bonded ring with folding of the backbone (DMSO and water) or a 5-membered NαH─αCO (water) to stabilize E-type rotamers. Such aza-PNA oligomers with exclusive E rotamers and intraresidue backbone H-bonding can modulate its DNA/RNA binding and assembling properties.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectAmidesen_US
dc.subjectChemical structureen_US
dc.subjectNuclear magnetic resonance spectroscopyen_US
dc.subjectOrganic compoundsen_US
dc.subjectSolventsen_US
dc.subject2022-DEC-WEEK3en_US
dc.subjectTOC-DEC-2022en_US
dc.subject2022en_US
dc.titleAza-PNA: Engineering E-Rotamer Selectivity Directed by Intramolecular H-bondingen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleOrganic Lettersen_US
dc.publication.originofpublisherForeignen_US
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