AbstractThe synthesis of 1,2,3-triazoles was developed employing sequential copper azide–alkyne cycloaddition, tosylation, sodium azide, and copper azide–alkyne steps. This approach allowed the synthesis of two and three 1,2,3-triazole rings. A preliminary study to gain further insight into the reaction was performed using in situ ReactIR technology
The synthesis of N1 and N2 coumarin substituted 1,2,3-triazole isomers from terminal alkynes, sodium...
A facile and simple protocol for the ‘Click\u27 cycloaddition of organic azides with N-propargylchlo...
The nucleophilic substitution of benzylic bromides with sodium azide was combined with a subsequent ...
AbstractWe have developed an efficient method for the synthesis of functionalized C-glycosyl 1,2,3-t...
1,4-disubstituted 1,2,3-triazoles are obtained in high yields via one-pot three components reaction ...
The reaction of 1-alkynes with acylazides in the presence of [Tpm*,BrCu(NCMe)]BF4 (Tpm*,Br = tris(3,...
A one-pot protocol for the synthesis of 1,2,3-triazoles has been developed starting from inactivated...
Copper(I) oxide has been found to effectively catalyse the multicomponent click synthesis of fully s...
A scalable metal-, azide-, and halogen-free method for the synthesis of substituted 1,2,3-triazoles ...
The 15th International Electronic Conference on Synthetic Organic Chemistry session General Organic ...
AbstractHerein we report an approach to the formation of 5-alkynyl-1,3-dioxin-4-ones using Suzuki–Mi...
Micellar media in water provide a simple and efficient environment to favor the multi-component synt...
This thesis describes the synthetic approaches undertaken to generate various substituted 1,2,3-tria...
The copper-catalysed azide-alkyne cycloaddition (CuAAC) is a highly efficient reaction and is the co...
PD/BD 135555/2018 CO2usE-1801P.00867.1.01 (contract no. IST-ID/263/2019)The N-alkylation of 1,3,5-tr...
The synthesis of N1 and N2 coumarin substituted 1,2,3-triazole isomers from terminal alkynes, sodium...
A facile and simple protocol for the ‘Click\u27 cycloaddition of organic azides with N-propargylchlo...
The nucleophilic substitution of benzylic bromides with sodium azide was combined with a subsequent ...
AbstractWe have developed an efficient method for the synthesis of functionalized C-glycosyl 1,2,3-t...
1,4-disubstituted 1,2,3-triazoles are obtained in high yields via one-pot three components reaction ...
The reaction of 1-alkynes with acylazides in the presence of [Tpm*,BrCu(NCMe)]BF4 (Tpm*,Br = tris(3,...
A one-pot protocol for the synthesis of 1,2,3-triazoles has been developed starting from inactivated...
Copper(I) oxide has been found to effectively catalyse the multicomponent click synthesis of fully s...
A scalable metal-, azide-, and halogen-free method for the synthesis of substituted 1,2,3-triazoles ...
The 15th International Electronic Conference on Synthetic Organic Chemistry session General Organic ...
AbstractHerein we report an approach to the formation of 5-alkynyl-1,3-dioxin-4-ones using Suzuki–Mi...
Micellar media in water provide a simple and efficient environment to favor the multi-component synt...
This thesis describes the synthetic approaches undertaken to generate various substituted 1,2,3-tria...
The copper-catalysed azide-alkyne cycloaddition (CuAAC) is a highly efficient reaction and is the co...
PD/BD 135555/2018 CO2usE-1801P.00867.1.01 (contract no. IST-ID/263/2019)The N-alkylation of 1,3,5-tr...
The synthesis of N1 and N2 coumarin substituted 1,2,3-triazole isomers from terminal alkynes, sodium...
A facile and simple protocol for the ‘Click\u27 cycloaddition of organic azides with N-propargylchlo...
The nucleophilic substitution of benzylic bromides with sodium azide was combined with a subsequent ...