An ultrarapid visible-light-driven method for catalyst-free ligation is reported. In their Communication on page 10284 ff., C. Barner-Kowollik and co-workers describe a highly efficient conjugation between an azirine moiety (white) and diverse dipolarophiles (red) under irradiation from blue LEDs. Following the photogeneration of a nitrile ylide (cyan structure), complete conversion into the cycloadduct takes place through a click-type reaction
The overwhelming success of click chemistry encouraged researchers to develop alternative "spring-lo...
This research synthesised and explored the application of novel chemicals which can be used to creat...
The current study introduces a tetrazole species able to perform a rapid, visible light induced nitr...
A rapid and catalyst-free cycloaddition system for visible-light-induced click chemistry is reported...
A rapid and catalyst-free cycloaddition system for visible-light-induced click chemistry is reported...
Photoclick chemistry represents a class of photo-activated click reactions generally characterised b...
Shining a light on click chemistry: The use of UV-radiation as trigger signal provides a facile mean...
Herein, we document the design and development of a novel (3 + 2) cycloaddition reaction aided by th...
The overwhelming success of click chemistry encouraged researchers to develop alternative spring-lo...
The overwhelming success of click chemistry encouraged researchers to develop alternative "spring-lo...
The overwhelming success of click chemistry encouraged researchers to develop alternative "spring-lo...
The overwhelming success of click chemistry encouraged researchers to develop alternative "spring-lo...
The overwhelming success of click chemistry encouraged researchers to develop alternative "spring-lo...
The simple and fast CLICK reaction, in which an azide is linked to an alkyne, has been used extensiv...
The overwhelming success of click chemistry encouraged researchers to develop alternative "spring-lo...
The overwhelming success of click chemistry encouraged researchers to develop alternative "spring-lo...
This research synthesised and explored the application of novel chemicals which can be used to creat...
The current study introduces a tetrazole species able to perform a rapid, visible light induced nitr...
A rapid and catalyst-free cycloaddition system for visible-light-induced click chemistry is reported...
A rapid and catalyst-free cycloaddition system for visible-light-induced click chemistry is reported...
Photoclick chemistry represents a class of photo-activated click reactions generally characterised b...
Shining a light on click chemistry: The use of UV-radiation as trigger signal provides a facile mean...
Herein, we document the design and development of a novel (3 + 2) cycloaddition reaction aided by th...
The overwhelming success of click chemistry encouraged researchers to develop alternative spring-lo...
The overwhelming success of click chemistry encouraged researchers to develop alternative "spring-lo...
The overwhelming success of click chemistry encouraged researchers to develop alternative "spring-lo...
The overwhelming success of click chemistry encouraged researchers to develop alternative "spring-lo...
The overwhelming success of click chemistry encouraged researchers to develop alternative "spring-lo...
The simple and fast CLICK reaction, in which an azide is linked to an alkyne, has been used extensiv...
The overwhelming success of click chemistry encouraged researchers to develop alternative "spring-lo...
The overwhelming success of click chemistry encouraged researchers to develop alternative "spring-lo...
This research synthesised and explored the application of novel chemicals which can be used to creat...
The current study introduces a tetrazole species able to perform a rapid, visible light induced nitr...