A series of strained alkynes, based on the 2,2’-dihydroxy-1,1’-biaryl structure, were prepared in a short sequence from readily-available starting materials. These compounds can be readily converted into further derivatives including examples containing fluorescent groups with potential for use as labelling reagents. The alkynes are able to react in cycloadditions with a range of azides without the requirement for a copper catalyst, in clean reactions with no observable side reactions
Alkynes are actually basic chemicals, serving as privileged synthons for planning new organic reacti...
A new class of macrocyclic angle-strained alkynes whose size and reactivity can be precisely tuned b...
Naturally occurring heterocycles such as pyrones, dihydropyrones, and isocoumarins have proven to be...
A series of strained alkynes were prepared from 2,2′-dihydroxy-biaryls. Several were characterised b...
Strained alkynes, i.e., alkynes distorted from the ideal linear geometry, undergo cycloaddition reac...
We report the synthesis of a bipyridyl reagent containing a strained alkyne, which significantly res...
The novel “double strained alkyne” 3 has been prepared and evaluated in strain-promoted azide-alkyne...
We recently reported two unexplored reactivities of alkynes and azides. The first method reacts nuc...
Abstract Al-Omari, Mohammad Synthesis of Alkynes from Bi-3H-diazirin-3-yls: Trapping of Strained C...
We describe the development of TMTH-SulfoxImine (TMTHSI) as a superior click reagent. This reagent c...
Improving the synthesis of complex organic molecules is essential for progress in many fields such a...
With the goal of identifying alkyne-like reagents for use in click chemistry, but without Cu catalys...
A nearly forgotten reaction discovered more than 60 years ago—the cycloaddition of a cyclic alkyne a...
The spontaneous activation of a nonaromatic enediynyl azide under ambient conditions has been demons...
Among all functional groups, alkynes occupy a privileged position in synthetic and medicinal chemist...
Alkynes are actually basic chemicals, serving as privileged synthons for planning new organic reacti...
A new class of macrocyclic angle-strained alkynes whose size and reactivity can be precisely tuned b...
Naturally occurring heterocycles such as pyrones, dihydropyrones, and isocoumarins have proven to be...
A series of strained alkynes were prepared from 2,2′-dihydroxy-biaryls. Several were characterised b...
Strained alkynes, i.e., alkynes distorted from the ideal linear geometry, undergo cycloaddition reac...
We report the synthesis of a bipyridyl reagent containing a strained alkyne, which significantly res...
The novel “double strained alkyne” 3 has been prepared and evaluated in strain-promoted azide-alkyne...
We recently reported two unexplored reactivities of alkynes and azides. The first method reacts nuc...
Abstract Al-Omari, Mohammad Synthesis of Alkynes from Bi-3H-diazirin-3-yls: Trapping of Strained C...
We describe the development of TMTH-SulfoxImine (TMTHSI) as a superior click reagent. This reagent c...
Improving the synthesis of complex organic molecules is essential for progress in many fields such a...
With the goal of identifying alkyne-like reagents for use in click chemistry, but without Cu catalys...
A nearly forgotten reaction discovered more than 60 years ago—the cycloaddition of a cyclic alkyne a...
The spontaneous activation of a nonaromatic enediynyl azide under ambient conditions has been demons...
Among all functional groups, alkynes occupy a privileged position in synthetic and medicinal chemist...
Alkynes are actually basic chemicals, serving as privileged synthons for planning new organic reacti...
A new class of macrocyclic angle-strained alkynes whose size and reactivity can be precisely tuned b...
Naturally occurring heterocycles such as pyrones, dihydropyrones, and isocoumarins have proven to be...