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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Pant, Debi D. | - |
dc.date.accessioned | 2024-02-08T04:29:19Z | - |
dc.date.available | 2024-02-08T04:29:19Z | - |
dc.date.issued | 2015-04 | - |
dc.identifier.uri | https://www.publish.csiro.au/ch/CH14708 | - |
dc.identifier.uri | http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/14099 | - |
dc.description.abstract | Fluorophores based on 4-triazolyl, 7-hydroxy-4-triazolylmethyl, 4-O-triazolylmethyl, and 7-O-triazolylmethyl coumaryl-tagged amino acids and dipeptides were synthesized by copper-catalyzed [3 + 2] cycloaddition reaction between azido- or alkynyl-functionalized coumarins with alkynyl- or azido-functionalized amino acid and dipeptides in good-to-excellent yields. Steady-state absorption and the fluorescence properties of the synthesized conjugates were studied. The chemical applicability of these amino acid and peptide-based fluorophores was successfully demonstrated by their linear elongation by further tagging them with appropriate C- or N-terminus amino acid. | en_US |
dc.language.iso | en | en_US |
dc.publisher | CSIRO | en_US |
dc.subject | Physics | en_US |
dc.subject | Amino acids | en_US |
dc.subject | Dipeptides | en_US |
dc.subject | Synthesis | en_US |
dc.subject | Absorption | en_US |
dc.title | Synthesis, Absorption, and Fluorescence Studies of Coumaryl-Labelled Amino Acids and Dipeptides Linked Via Triazole Ring | en_US |
dc.type | Article | en_US |
Appears in Collections: | Department of Physics |
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