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 |