A novel bioconjugation strategy is presented that relies on the coupling of diazonium terephthalates with amines in proteins. The diazonium captures the amine while the vicinal ester locks it through cyclization, ensuring no reversibility. The reaction is highly efficient and proceeds under mild conditions and short reaction times. Densely functionalized, complex natural products were directly coupled to proteins using low concentrations of coupling partners
Aryl transfer reactions from arenediazonium salts have started to make their impact in chemical biol...
For the first time, a simple methodology for the chemical synthesis and use of highly reactive 4-met...
A highly efficient protein bioconjugation method is described involving addition of anilines to o-am...
The field of bioconjugate chemistry is expansive and rapidly evolving, perennially introducing new s...
Bioconjugation is an important tool for studying complex biological systems, with site-specificity b...
In chemical biology, azides are used to chemically manipulate target structures in a bioorthogonal m...
Aryl diazonium cations are versatile bioconjugation reagents due to their reactivity towards electro...
Unnatural amino acid technologies have been critical in introducing unique chemical functionality to...
In chemical biology, azides are used to chemically manipulate target structures in a bioorthogonal m...
The development of novel bioconjugation strategies for the functionalisation of polypeptides and pro...
A large variety of biomolecules such as lipids, DNA, carbohydrates and proteins exist inside cells. ...
The incorporation of non-canonical amino acids introduces unique chemical functionality to proteins,...
An unprecedented condensation reaction of N-benzylimines was applied to the bioconjugation of lysine...
Advances in bioconjugation, the ability to link biomolecules to each other, small molecules, surface...
Aryl transfer reactions from arenediazonium salts have started to make their impact in chemical biol...
For the first time, a simple methodology for the chemical synthesis and use of highly reactive 4-met...
A highly efficient protein bioconjugation method is described involving addition of anilines to o-am...
The field of bioconjugate chemistry is expansive and rapidly evolving, perennially introducing new s...
Bioconjugation is an important tool for studying complex biological systems, with site-specificity b...
In chemical biology, azides are used to chemically manipulate target structures in a bioorthogonal m...
Aryl diazonium cations are versatile bioconjugation reagents due to their reactivity towards electro...
Unnatural amino acid technologies have been critical in introducing unique chemical functionality to...
In chemical biology, azides are used to chemically manipulate target structures in a bioorthogonal m...
The development of novel bioconjugation strategies for the functionalisation of polypeptides and pro...
A large variety of biomolecules such as lipids, DNA, carbohydrates and proteins exist inside cells. ...
The incorporation of non-canonical amino acids introduces unique chemical functionality to proteins,...
An unprecedented condensation reaction of N-benzylimines was applied to the bioconjugation of lysine...
Advances in bioconjugation, the ability to link biomolecules to each other, small molecules, surface...
Aryl transfer reactions from arenediazonium salts have started to make their impact in chemical biol...
For the first time, a simple methodology for the chemical synthesis and use of highly reactive 4-met...
A highly efficient protein bioconjugation method is described involving addition of anilines to o-am...