We describe the development of TMTH-SulfoxImine (TMTHSI) as a superior click reagent. This reagent combines a great reactivity, with small size and low hydrophobicity and compares outstandingly with existing click reagents. TMTHSI can be conveniently functionalized with a variety of linkers allowing attachment of a diversity of small molecules and (peptide, nucleic acid) biologics
We report the synthesis of a bipyridyl reagent containing a strained alkyne, which significantly res...
The Cu-catalysed alkyne-azide cycloaddition (CuAAC) or 'click' reaction is a powerful and robust bio...
The overwhelming success of click chemistry encouraged researchers to develop alternative spring-lo...
We describe the development of TMTH-SulfoxImine (TMTHSI) as a superior click reagent. This reagent c...
The site specific attachment of the reactive TMTHSI-click handle to the N-terminus of peptides and p...
The recently developed compound, tetramethylthiocycloheptyne sulfoximine (TMTHSI), has shown to be a...
ABSTRACT: The alkyne-azide cycloaddition, popularly known as the "click" reaction, has been extensiv...
The need for precise and flexible synthetic methodology to underpin modern research in chemical biol...
We recently reported two unexplored reactivities of alkynes and azides. The first method reacts nuc...
Strained alkynes, i.e., alkynes distorted from the ideal linear geometry, undergo cycloaddition reac...
The reaction of triazolinediones (TADs) and indoles is of particular interest for polymer chemistry ...
With the goal of identifying alkyne-like reagents for use in click chemistry, but without Cu catalys...
Conjugation of ligands to DNA oligonucleotides has been achieved in the solid phase by strain-promot...
A series of strained alkynes, based on the 2,2’-dihydroxy-1,1’-biaryl structure, were prepared in a ...
Among all functional groups, alkynes occupy a privileged position in synthetic and medicinal chemist...
We report the synthesis of a bipyridyl reagent containing a strained alkyne, which significantly res...
The Cu-catalysed alkyne-azide cycloaddition (CuAAC) or 'click' reaction is a powerful and robust bio...
The overwhelming success of click chemistry encouraged researchers to develop alternative spring-lo...
We describe the development of TMTH-SulfoxImine (TMTHSI) as a superior click reagent. This reagent c...
The site specific attachment of the reactive TMTHSI-click handle to the N-terminus of peptides and p...
The recently developed compound, tetramethylthiocycloheptyne sulfoximine (TMTHSI), has shown to be a...
ABSTRACT: The alkyne-azide cycloaddition, popularly known as the "click" reaction, has been extensiv...
The need for precise and flexible synthetic methodology to underpin modern research in chemical biol...
We recently reported two unexplored reactivities of alkynes and azides. The first method reacts nuc...
Strained alkynes, i.e., alkynes distorted from the ideal linear geometry, undergo cycloaddition reac...
The reaction of triazolinediones (TADs) and indoles is of particular interest for polymer chemistry ...
With the goal of identifying alkyne-like reagents for use in click chemistry, but without Cu catalys...
Conjugation of ligands to DNA oligonucleotides has been achieved in the solid phase by strain-promot...
A series of strained alkynes, based on the 2,2’-dihydroxy-1,1’-biaryl structure, were prepared in a ...
Among all functional groups, alkynes occupy a privileged position in synthetic and medicinal chemist...
We report the synthesis of a bipyridyl reagent containing a strained alkyne, which significantly res...
The Cu-catalysed alkyne-azide cycloaddition (CuAAC) or 'click' reaction is a powerful and robust bio...
The overwhelming success of click chemistry encouraged researchers to develop alternative spring-lo...