Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/9904
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dc.contributor.authorRasale, Dnyaneshwar B.en_US
dc.contributor.authorMaity, Indrajiten_US
dc.contributor.authorDas, Apurba Kumaren_US
dc.date.accessioned2022-05-05T15:51:40Z-
dc.date.available2022-05-05T15:51:40Z-
dc.date.issued2014-
dc.identifier.citationRasale, D. B., Maity, I., & Das, A. K. (2014). In situ generation of redox active peptides driven by selenoester mediated native chemical ligation. Chemical Communications, 50(77), 1139711400. https://doi.org/10.1039/C4CC03835Een_US
dc.identifier.issn1359-7345-
dc.identifier.otherEID(2-s2.0-84907075325)-
dc.identifier.urihttps://doi.org/10.1039/c4cc03835e-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/9904-
dc.description.abstractRedox active peptides are generated through selenoester mediated native chemical ligation (NCL). Distinct nanostructures, such as nanotubes to nanofibrillar architectures, were observed for self-assembling soft materials. © 2014 The Partner Organisations.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.sourceChemical Communicationsen_US
dc.subjectcysteinylglycine|dipeptide|disulfide|ester|nanomaterial|oxidizing agent|peptide|selenium derivative|ester|nanotube|peptide|redox active peptide|selenoester|unclassified drug|atomic force microscopy|chemistry|oxidation reduction reaction|synthesis|ultrastructure|article|chemical reaction|gel|high performance liquid chromatography|hydrogen bond|native chemical ligation|oxidation reduction reaction|phase transition|protein conformation|protein synthesis|Dipeptides|Disulfides|Esters|Microscopy, Atomic Force|Nanostructures|Oxidants|Oxidation-Reduction|Peptides|Selenium Compoundsen_US
dc.titleIn situ generation of redox active peptides driven by selenoester mediated native chemical ligationen_US
dc.typeJournal Articleen_US
Appears in Collections:Department of Chemistry

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