Development of a tandem ‘click-click’ approach to the formation of successive 1,4-disubstituted 1,2,3-triazole linkages and ‘click chemistry’ on sugar-derived alkynes are described
1,2,3-Triazoles find applications in several major technological areas, and especially in drug disco...
The copper(I)-catalyzed modern version of the Huisgen-type azide–alkyne cycloaddition to give a 1,4...
This thesis describes the synthetic approaches undertaken to generate various substituted 1,2,3-tria...
Development of a tandem 'click-click' approach to the formation of successive 1,4-disubstituted 1,2,...
The click concept, as originally discussed by Sharpless, Finn, and Kolb, is both powerful and simple...
Nowadays, the click reaction of azides with alkynes has evolved rapidly and become one of the most e...
In the last years, we have investigated the click-chemical space covered by molecules containing the...
The preparation of several alkynyl esters, derived from amino acids, coumarins and an alkynyl deriva...
(English) Charles University Faculty of Pharmacy in Hradec Králové Department of Pharmaceutical Chem...
1,2,3-Triazoles, which can be readily prepared from click chemistry, are important building componen...
A three-component coupling was used to prepare a series of 1,4-disubstituted-1,2,3-triazoles from th...
Abstract: The synthesis of a series of novel 1,4-disubstituted 1,2,3-triazole compounds bearing a D-...
Accepted author version posted online: 05 Jun 2012The synthesis of a series of novel 1,4-disubstitut...
Glycosyl azides, prepared in situ from glucal and trimethylsilyl azide via Ferrier rearrangement, un...
The Cu(I)-catalyzed azide-alkyne cycloaddition reaction, also known as click chemistry, has become a...
1,2,3-Triazoles find applications in several major technological areas, and especially in drug disco...
The copper(I)-catalyzed modern version of the Huisgen-type azide–alkyne cycloaddition to give a 1,4...
This thesis describes the synthetic approaches undertaken to generate various substituted 1,2,3-tria...
Development of a tandem 'click-click' approach to the formation of successive 1,4-disubstituted 1,2,...
The click concept, as originally discussed by Sharpless, Finn, and Kolb, is both powerful and simple...
Nowadays, the click reaction of azides with alkynes has evolved rapidly and become one of the most e...
In the last years, we have investigated the click-chemical space covered by molecules containing the...
The preparation of several alkynyl esters, derived from amino acids, coumarins and an alkynyl deriva...
(English) Charles University Faculty of Pharmacy in Hradec Králové Department of Pharmaceutical Chem...
1,2,3-Triazoles, which can be readily prepared from click chemistry, are important building componen...
A three-component coupling was used to prepare a series of 1,4-disubstituted-1,2,3-triazoles from th...
Abstract: The synthesis of a series of novel 1,4-disubstituted 1,2,3-triazole compounds bearing a D-...
Accepted author version posted online: 05 Jun 2012The synthesis of a series of novel 1,4-disubstitut...
Glycosyl azides, prepared in situ from glucal and trimethylsilyl azide via Ferrier rearrangement, un...
The Cu(I)-catalyzed azide-alkyne cycloaddition reaction, also known as click chemistry, has become a...
1,2,3-Triazoles find applications in several major technological areas, and especially in drug disco...
The copper(I)-catalyzed modern version of the Huisgen-type azide–alkyne cycloaddition to give a 1,4...
This thesis describes the synthetic approaches undertaken to generate various substituted 1,2,3-tria...
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