A site-specific and efficient method for N-terminal modification of peptides using oxone for selective oxidation of N-terminal α-amino groups of peptides to oximes followed by transoximation with O-substituted hydroxylamines has been developed.Department of Applied Biology and Chemical Technolog
With use ofmethyl(trifluoromethyl)dioxirane (TFDO), the oxidation of some tripeptide esters protecte...
A method of highly selective N-terminal modification of proteins as well as peptides by an isolated ...
The hydroxyl radical-mediated oxidation of peptides and proteins constitutes a large group of post-t...
Use of oxime forming reactions has become a widely applied strategy for peptide and protein bioconju...
ABSTRACT: The synthetic modification of proteins plays an important role in chemical biology and bio...
PolyU Library Call No.: [THS] LG51 .H577M ABCT 2015 Wongxxiv, 191 pages :color illustrationsAldehyde...
The synthetic modification of proteins plays an important role in chemical biology and biomaterials ...
The goal of protein modification is to take advantage of the structural complexity and bindingspecif...
A new method for oxidative synthesis of amides from alkynes and amines in high yields (up to 96%) us...
Mild oxidation with periodate of the 1-amino-2-ol moiety of N-terminal seryl or threonyl peptides an...
Because almost all peptides and proteins have only one N- and one C-terminus, modification targeting...
Mild conditions for oxime ligations via in situ generation of α-imino amide intermediates are report...
The controlled attachment of synthetic groups to proteins is important for a number of fields, inclu...
As applications of protein-based materials become increasingly complex, there is a growing need for ...
A direct method for the transformation of α-amino acids into β-amino aldehydes was developed, and ap...
With use ofmethyl(trifluoromethyl)dioxirane (TFDO), the oxidation of some tripeptide esters protecte...
A method of highly selective N-terminal modification of proteins as well as peptides by an isolated ...
The hydroxyl radical-mediated oxidation of peptides and proteins constitutes a large group of post-t...
Use of oxime forming reactions has become a widely applied strategy for peptide and protein bioconju...
ABSTRACT: The synthetic modification of proteins plays an important role in chemical biology and bio...
PolyU Library Call No.: [THS] LG51 .H577M ABCT 2015 Wongxxiv, 191 pages :color illustrationsAldehyde...
The synthetic modification of proteins plays an important role in chemical biology and biomaterials ...
The goal of protein modification is to take advantage of the structural complexity and bindingspecif...
A new method for oxidative synthesis of amides from alkynes and amines in high yields (up to 96%) us...
Mild oxidation with periodate of the 1-amino-2-ol moiety of N-terminal seryl or threonyl peptides an...
Because almost all peptides and proteins have only one N- and one C-terminus, modification targeting...
Mild conditions for oxime ligations via in situ generation of α-imino amide intermediates are report...
The controlled attachment of synthetic groups to proteins is important for a number of fields, inclu...
As applications of protein-based materials become increasingly complex, there is a growing need for ...
A direct method for the transformation of α-amino acids into β-amino aldehydes was developed, and ap...
With use ofmethyl(trifluoromethyl)dioxirane (TFDO), the oxidation of some tripeptide esters protecte...
A method of highly selective N-terminal modification of proteins as well as peptides by an isolated ...
The hydroxyl radical-mediated oxidation of peptides and proteins constitutes a large group of post-t...