Glycosyl azides, prepared in situ from glucal and trimethylsilyl azide via Ferrier rearrangement, undergo smooth coupling with alkynes under neutral conditions by means of 'Click reactions' to furnish 1,2,3-triazole-linked glycoconjugates in high yields and with moderate stereoselectivity. The method provides a convenient route to prepare glycoconjugates from glucals, trimethylsilyl azide, and alkynes via a three component reaction
A three-component coupling was used to prepare a series of 1,4-disubstituted-1,2,3-triazoles from th...
Carbohydrate–triazole conjugates proved themselves as valuable enzyme activity-modifying agents. Rec...
2-Azidoalcohols derived in situ from epoxides and sodium azide undergo smooth coupling with alkynes ...
We have developed an efficient method for the synthesis of functionalized C-glycosyl 1,2,3-triazoles...
AbstractWe have developed an efficient method for the synthesis of functionalized C-glycosyl 1,2,3-t...
We have developed an efficient method for the synthesis of functionalized C-glycosyl 1,2,3-triazoles...
Abstract: The synthesis of a series of novel 1,4-disubstituted 1,2,3-triazole compounds bearing a D-...
The preparation of several alkynyl esters, derived from amino acids, coumarins and an alkynyl deriva...
We have explored the synthesis of various triazole-containing glycoconjugates with gluco-, allo-, ga...
The preparation of several alkynyl esters, derived from amino acids, coumarins and an alkynyl deriva...
The synthetic methodology and experimental results concerning to the preparation of glycoconjugates ...
Nowadays, the click reaction of azides with alkynes has evolved rapidly and become one of the most e...
The copper(I)-catalyzed modern version of the Huisgen-type azide–alkyne cycloaddition to give a 1,4...
Development of a tandem 'click-click' approach to the formation of successive 1,4-disubstituted 1,2,...
Carbohydrate–triazole conjugates proved themselves as valuable enzyme activity-modifying agents. Rec...
A three-component coupling was used to prepare a series of 1,4-disubstituted-1,2,3-triazoles from th...
Carbohydrate–triazole conjugates proved themselves as valuable enzyme activity-modifying agents. Rec...
2-Azidoalcohols derived in situ from epoxides and sodium azide undergo smooth coupling with alkynes ...
We have developed an efficient method for the synthesis of functionalized C-glycosyl 1,2,3-triazoles...
AbstractWe have developed an efficient method for the synthesis of functionalized C-glycosyl 1,2,3-t...
We have developed an efficient method for the synthesis of functionalized C-glycosyl 1,2,3-triazoles...
Abstract: The synthesis of a series of novel 1,4-disubstituted 1,2,3-triazole compounds bearing a D-...
The preparation of several alkynyl esters, derived from amino acids, coumarins and an alkynyl deriva...
We have explored the synthesis of various triazole-containing glycoconjugates with gluco-, allo-, ga...
The preparation of several alkynyl esters, derived from amino acids, coumarins and an alkynyl deriva...
The synthetic methodology and experimental results concerning to the preparation of glycoconjugates ...
Nowadays, the click reaction of azides with alkynes has evolved rapidly and become one of the most e...
The copper(I)-catalyzed modern version of the Huisgen-type azide–alkyne cycloaddition to give a 1,4...
Development of a tandem 'click-click' approach to the formation of successive 1,4-disubstituted 1,2,...
Carbohydrate–triazole conjugates proved themselves as valuable enzyme activity-modifying agents. Rec...
A three-component coupling was used to prepare a series of 1,4-disubstituted-1,2,3-triazoles from th...
Carbohydrate–triazole conjugates proved themselves as valuable enzyme activity-modifying agents. Rec...
2-Azidoalcohols derived in situ from epoxides and sodium azide undergo smooth coupling with alkynes ...