Triazolinediones (TADs) are unique reagents in organic synthesis that have also found wide applications in different research disciplines, in spite of their somewhat "exotic" reputation. In this review, we offer two case studies that demonstrate the possibilities of these versatile and reliable synthetic tools, namely, in the field of polymer science as well as in more recently emerging applications in the field of click chemistry. As the general use of triazolinediones has always been hampered by the limited commercial and synthetic availability of such reagents, we also offer a review of the available TAD reagents, together with a detailed discussion of their synthesis and reactivity. This review thus aims to serve as a practical guide fo...
The multi-gram synthesis of a wide range of 1,2,3-triazolines via azide–alkene cycloaddition reactio...
This study illustrates the utility of click chemistry in functionalizing triazabutadienes by allowin...
Nowadays, the click reaction of azides with alkynes has evolved rapidly and become one of the most e...
Triazolinediones (TADs) are unique reagents in organic synthesis that have also found wide applicati...
The reaction of triazolinediones (TADs) and indoles is of particular interest for polymer chemistry ...
In the last few years, heterocyclic compounds have attracted strong interest and a lot of work has b...
The donor ortho-dimethyl-TTF-(N-n-Bu-1,2,3-triazole) 1,5-isomer has been synthesized by click chemis...
AbstractSeveral triazonine-carbaldehyde derivatives have been prepared using different protocols; ho...
With its focus on synthetic reactions that are highly specific and reliable, 'click' chemistry has b...
Heterocyclic chemistry is fundamental to biology and medicine. It is not implausible to say that we ...
A general method for the synthesis of 1,3,5-trisubstituted 1,2,4-triazoles has been developed from r...
Multicomponent, solid-phase, microwave and grinding methods are the constructive modes in the sustai...
In a wide rang1ng reaction dimethyl diazomalonate reacted with pr1mary amines to yield the correspon...
Previously held under moratorium in Chemistry Department (GSK) from 17/06/2020 until 22/11/2022New m...
Over the past decade, organocatalytic synthetic procedures have emerged as an essential part of tria...
The multi-gram synthesis of a wide range of 1,2,3-triazolines via azide–alkene cycloaddition reactio...
This study illustrates the utility of click chemistry in functionalizing triazabutadienes by allowin...
Nowadays, the click reaction of azides with alkynes has evolved rapidly and become one of the most e...
Triazolinediones (TADs) are unique reagents in organic synthesis that have also found wide applicati...
The reaction of triazolinediones (TADs) and indoles is of particular interest for polymer chemistry ...
In the last few years, heterocyclic compounds have attracted strong interest and a lot of work has b...
The donor ortho-dimethyl-TTF-(N-n-Bu-1,2,3-triazole) 1,5-isomer has been synthesized by click chemis...
AbstractSeveral triazonine-carbaldehyde derivatives have been prepared using different protocols; ho...
With its focus on synthetic reactions that are highly specific and reliable, 'click' chemistry has b...
Heterocyclic chemistry is fundamental to biology and medicine. It is not implausible to say that we ...
A general method for the synthesis of 1,3,5-trisubstituted 1,2,4-triazoles has been developed from r...
Multicomponent, solid-phase, microwave and grinding methods are the constructive modes in the sustai...
In a wide rang1ng reaction dimethyl diazomalonate reacted with pr1mary amines to yield the correspon...
Previously held under moratorium in Chemistry Department (GSK) from 17/06/2020 until 22/11/2022New m...
Over the past decade, organocatalytic synthetic procedures have emerged as an essential part of tria...
The multi-gram synthesis of a wide range of 1,2,3-triazolines via azide–alkene cycloaddition reactio...
This study illustrates the utility of click chemistry in functionalizing triazabutadienes by allowin...
Nowadays, the click reaction of azides with alkynes has evolved rapidly and become one of the most e...