In the last years, we have investigated the click-chemical space covered by molecules containing the triazole ring and generated a database of 1,2,3-triazoles called ZINClick, starting from literature-reported alkynes and azides synthesizable in no more than three synthetic steps from commercially available products. This combinatorial database contains millions of 1,4-disubstituted 1,2,3-triazoles that are easily synthesizable. The library is regularly updated and can be freely downloaded from http://www.ZINClick.org . In this communication, the new implementation of ZINClick will be discussed as well as our new strategy for clustering the chemical space covered by 1,4-disubstituted 1,2,3-triazoles around their availability: from direct pu...
The click concept, as originally discussed by Sharpless, Finn, and Kolb, is both powerful and simple...
A mild method for regioselective formation of 1,5-substituted 1,2,3-triazoles is described. The zinc...
Development of a tandem ‘click-click’ approach to the formation of successive 1,4-disubstituted 1,2,...
In the last years, we have investigated the click-chemical space covered by molecules containing the...
In the last years, we have investigated the click-chemical space covered by molecules containing the...
This chapter provides a brief overview of the applications of ZINClick virtual library. In the last ...
1,2,3-Triazoles, which can be readily prepared from click chemistry, are important building componen...
Combinatorial chemistry has become an extremely power-ful technique for the rapid generation of smal...
After 20 years since its conception, click chemistry has come of age and we believe the time has com...
Nowadays, the click reaction of azides with alkynes has evolved rapidly and become one of the most e...
(English) Charles University Faculty of Pharmacy in Hradec Králové Department of Pharmaceutical Chem...
Over the past decade, organocatalytic synthetic procedures have emerged as an essential part of tria...
The heterocyclic family of azoles have recently become one of the most widely used members of the N-...
[Figure not available: see fulltext.][Figure not available: see fulltext.]Microreview summarizes the...
1,2,3-Triazoles find applications in several major technological areas, and especially in drug disco...
The click concept, as originally discussed by Sharpless, Finn, and Kolb, is both powerful and simple...
A mild method for regioselective formation of 1,5-substituted 1,2,3-triazoles is described. The zinc...
Development of a tandem ‘click-click’ approach to the formation of successive 1,4-disubstituted 1,2,...
In the last years, we have investigated the click-chemical space covered by molecules containing the...
In the last years, we have investigated the click-chemical space covered by molecules containing the...
This chapter provides a brief overview of the applications of ZINClick virtual library. In the last ...
1,2,3-Triazoles, which can be readily prepared from click chemistry, are important building componen...
Combinatorial chemistry has become an extremely power-ful technique for the rapid generation of smal...
After 20 years since its conception, click chemistry has come of age and we believe the time has com...
Nowadays, the click reaction of azides with alkynes has evolved rapidly and become one of the most e...
(English) Charles University Faculty of Pharmacy in Hradec Králové Department of Pharmaceutical Chem...
Over the past decade, organocatalytic synthetic procedures have emerged as an essential part of tria...
The heterocyclic family of azoles have recently become one of the most widely used members of the N-...
[Figure not available: see fulltext.][Figure not available: see fulltext.]Microreview summarizes the...
1,2,3-Triazoles find applications in several major technological areas, and especially in drug disco...
The click concept, as originally discussed by Sharpless, Finn, and Kolb, is both powerful and simple...
A mild method for regioselective formation of 1,5-substituted 1,2,3-triazoles is described. The zinc...
Development of a tandem ‘click-click’ approach to the formation of successive 1,4-disubstituted 1,2,...