AbstractPeptide thioesters are important tools for the total synthesis of proteins using native chemical ligation (NCL). Preparation of glycopeptide thioesters, that enable the assembly of homogeneously glycosylated proteins, is complicated by the perceived fragile nature of the sugar moiety. Herein, we demonstrate the compatibility of thioester formation via N→S acyl transfer with native N-glycopeptides and report observations that will aid in their preparation
Since the discovery of native chemical ligation (NCL) by Kent and coworkers in 1994, the field of pe...
Total synthesis of native and functional proteins was almost unachievable back in the early 1990s, b...
Total synthesis of native and functional proteins was almost unachievable back in the early 1990s, b...
AbstractPeptide thioesters are important tools for the total synthesis of proteins using native chem...
The broad utility of native chemical ligation (NCL) in protein synthesis has fostered a search for m...
The broad utility of native chemical ligation (NCL) in protein synthesis has fostered a search for m...
It is not highly sophisticated, yet the N→S acyl transfer reaction of a native peptide sequence pote...
Homogeneous, structurally defined glycoproteins can be assembled by coupling synthetic glycopeptides...
The thiol-ene ‘click’ reaction has emerged as a versatile process for carbon–sulfur bond formation w...
The thiol-ene ‘click’ reaction has emerged as a versatile process for carbon–sulfur bond formation w...
The thiol-ene ‘click’ reaction has emerged as a versatile process for carbon–sulfur bond formation w...
Proteins are synthesized only by living organisms. Today, we are able to receive them by recombinant...
We report on the photoinduced addition of glycosyl thiols to alkenyl glycines (thiol-ene coupling) t...
Glycoproteins consist of carbohydrates covalently linked with proteins. They are widely distributed ...
We report on the photoinduced addition of glycosyl thiols to alkenyl glycines (thiol–ene coupling) t...
Since the discovery of native chemical ligation (NCL) by Kent and coworkers in 1994, the field of pe...
Total synthesis of native and functional proteins was almost unachievable back in the early 1990s, b...
Total synthesis of native and functional proteins was almost unachievable back in the early 1990s, b...
AbstractPeptide thioesters are important tools for the total synthesis of proteins using native chem...
The broad utility of native chemical ligation (NCL) in protein synthesis has fostered a search for m...
The broad utility of native chemical ligation (NCL) in protein synthesis has fostered a search for m...
It is not highly sophisticated, yet the N→S acyl transfer reaction of a native peptide sequence pote...
Homogeneous, structurally defined glycoproteins can be assembled by coupling synthetic glycopeptides...
The thiol-ene ‘click’ reaction has emerged as a versatile process for carbon–sulfur bond formation w...
The thiol-ene ‘click’ reaction has emerged as a versatile process for carbon–sulfur bond formation w...
The thiol-ene ‘click’ reaction has emerged as a versatile process for carbon–sulfur bond formation w...
Proteins are synthesized only by living organisms. Today, we are able to receive them by recombinant...
We report on the photoinduced addition of glycosyl thiols to alkenyl glycines (thiol-ene coupling) t...
Glycoproteins consist of carbohydrates covalently linked with proteins. They are widely distributed ...
We report on the photoinduced addition of glycosyl thiols to alkenyl glycines (thiol–ene coupling) t...
Since the discovery of native chemical ligation (NCL) by Kent and coworkers in 1994, the field of pe...
Total synthesis of native and functional proteins was almost unachievable back in the early 1990s, b...
Total synthesis of native and functional proteins was almost unachievable back in the early 1990s, b...