dc.contributor.author |
Burilov V. |
|
dc.contributor.author |
Epifanova N. |
|
dc.contributor.author |
Popova E. |
|
dc.contributor.author |
Vasilevsky S. |
|
dc.contributor.author |
Solovieva S. |
|
dc.contributor.author |
Antipin I. |
|
dc.contributor.author |
Konovalov A. |
|
dc.date.accessioned |
2018-09-18T20:17:38Z |
|
dc.date.available |
2018-09-18T20:17:38Z |
|
dc.date.issued |
2013 |
|
dc.identifier.issn |
1066-5285 |
|
dc.identifier.uri |
https://dspace.kpfu.ru/xmlui/handle/net/138392 |
|
dc.description.abstract |
Regioselective synthesis of 1,2,3-triazolyl derivatives of calix[4]arenes based on the 1,3-dipolar cycloaddition of substituted benzyl azides to tetra(propargyloxy)calix[4]arenes in the presence of copper iodide was carried out. The presence of the p-methoxybenzyl substituent in the triazole ring leads to a dramatic (more than tenfold) increase in the fluorescence of the corresponding macrocycle in a region of 290-310 nm. © 2013 Springer Science+Business Media New York. |
|
dc.relation.ispartofseries |
Russian Chemical Bulletin |
|
dc.subject |
1,2,3-triazoles |
|
dc.subject |
1,3-dipolar cycloaddition |
|
dc.subject |
benzyl azides |
|
dc.subject |
calix[4]arenes |
|
dc.subject |
fluorescence |
|
dc.title |
Regioselective synthesis of 1,2,3-triazolyl derivatives of calix[4]arenes based on 1,3-dipolar cycloaddition |
|
dc.type |
Article |
|
dc.relation.ispartofseries-issue |
3 |
|
dc.relation.ispartofseries-volume |
62 |
|
dc.collection |
Публикации сотрудников КФУ |
|
dc.relation.startpage |
767 |
|
dc.source.id |
SCOPUS10665285-2013-62-3-SID84891815156 |
|