dc.contributor.author |
Sibgatullina R. |
|
dc.contributor.author |
Fujiki K. |
|
dc.contributor.author |
Murase T. |
|
dc.contributor.author |
Yamamoto T. |
|
dc.contributor.author |
Shimoda T. |
|
dc.contributor.author |
Kurbangalieva A. |
|
dc.contributor.author |
Tanaka K. |
|
dc.date.accessioned |
2018-09-19T22:00:10Z |
|
dc.date.available |
2018-09-19T22:00:10Z |
|
dc.date.issued |
2017 |
|
dc.identifier.issn |
0040-4039 |
|
dc.identifier.uri |
https://dspace.kpfu.ru/xmlui/handle/net/144576 |
|
dc.description.abstract |
© 2017 Elsevier LtdOne pot double click strategy containing strain-promoted click-reaction followed by 6π-azaelectrocyclization (RIKEN click reaction) has worked well in the synthesis of multivalent homogeneous and heterogeneous N-glycoalbumins. We have slightly changed the structure of linker unsaturated aldehyde used in this method. As a result it can be easily synthesized from commercially available material and furthermore, the enhancement of its reactivity towards both click-reactions was observed. The data described in this Communications facilitate the usage of the double click strategy as a general method for the synthesis of a variety of neo-N-glycoproteins. |
|
dc.relation.ispartofseries |
Tetrahedron Letters |
|
dc.subject |
Asparagine-linked glycans (N-glycans) |
|
dc.subject |
Glycoconjugation |
|
dc.subject |
Lysine |
|
dc.subject |
N-Glycoalbumin |
|
dc.subject |
RIKEN click reaction |
|
dc.title |
Highly reactive “RIKEN click” probe for glycoconjugation on lysines |
|
dc.type |
Article |
|
dc.relation.ispartofseries-issue |
20 |
|
dc.relation.ispartofseries-volume |
58 |
|
dc.collection |
Публикации сотрудников КФУ |
|
dc.relation.startpage |
1929 |
|
dc.source.id |
SCOPUS00404039-2017-58-20-SID85017559448 |
|