| dc.contributor.author |
Kumar, Anil |
|
| dc.date.accessioned |
2021-10-27T04:09:17Z |
|
| dc.date.available |
2021-10-27T04:09:17Z |
|
| dc.date.issued |
2013-03-14 |
|
| dc.identifier.uri |
https://onlinelibrary.wiley.com/doi/10.1002/chin.201312119 |
|
| dc.identifier.uri |
http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2914 |
|
| dc.description.abstract |
The archetypical CuAAC click chemistry is explored to assemble diverse 3-(triazol-1-yl)methyl-imidazo[1,2-a]pyridines. The approach is simple, general, and environmentally benign to generate a library of novel triazolo-imidazo[1,2-a]pyridine derivatives in good yield (30–90%). |
en_US |
| dc.language.iso |
en |
en_US |
| dc.publisher |
Wiley |
en_US |
| dc.subject |
Chemistry |
en_US |
| dc.subject |
ChemInform |
en_US |
| dc.subject |
CuAAC Reaction |
en_US |
| dc.subject |
Synthesis |
en_US |
| dc.title |
ChemInform Abstract: Exploration of the CuAAC Reaction for the Synthesis of Novel 3-(Triazol-1-yl)methyl-imidazo[1,2-a]pyridines |
en_US |
| dc.type |
Article |
en_US |