Developments and recent advancements in the field of endogenous amino acid selective bond forming reactions for bioconjugation.
about
A versatile platform for surface modification of microfluidic droplets.Selective N-terminal functionalization of native peptides and proteins.Chemical Protein Modification through Cysteine.Site-selective incorporation and ligation of protein aldehydes.Bioconjugation - using selective chemistry to enhance the properties of proteins and peptides as therapeutics and carriers.The Cysteine S-Alkylation Reaction as a Synthetic Method to Covalently Modify Peptide Sequences.Protein tetrazinylation via diazonium coupling for covalent and catalyst-free bioconjugation.A Facile Method for Preferential Modification of the N-Terminal Amino Group of Peptides Using Triazine-Based Coupling Reagents.Next-generation disulfide stapling: reduction and functional re-bridging all in one.Evaluation of Virus-Like Particle-Based Tumor-Associated Carbohydrate Immunogen in a Mouse Tumor Model.Gold-catalyzed direct alkynylation of tryptophan in peptides using TIPS-EBX.2-(Maleimidomethyl)-1,3-Dioxanes (MD): a Serum-Stable Self-hydrolysable Hydrophilic Alternative to Classical Maleimide ConjugationResidue-Specific Peptide Modification: A Chemist's Guide.Irreversible Protein Labeling by Paal-Knorr Conjugation.Redox-based reagents for chemoselective methionine bioconjugation.Chloromethyl-triazole: a new motif for site-selective pseudo-acylation of proteins.Palladium-Catalyzed Chemoselective and Biocompatible Functionalization of Cysteine-Containing Molecules at Room Temperature.Decarboxylative alkylation for site-selective bioconjugation of native proteins via oxidation potentials.Selective lysine modification of native peptides via aza-Michael addition.Fluorescent Nanodiamond-bacteriophage Conjugates Maintain Host Specificity.Palladium Oxidative Addition Complexes for Peptide and Protein Crosslinking.A convenient method for multicolour labelling of proteins with BODIPY fluorophores via tyrosine residues.Modification of Amino Groups.A protein functionalization platform based on selective reactions at methionine residuesRapid phenolic O-glycosylation of small molecules and complex unprotected peptides in aqueous solventIminoboronates are efficient intermediates for selective, rapid and reversible -terminal cysteine functionalisation
P2860
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P2860
Developments and recent advancements in the field of endogenous amino acid selective bond forming reactions for bioconjugation.
description
2015 nî lūn-bûn
@nan
2015年の論文
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2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
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2015年论文
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2015年论文
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name
Developments and recent advanc ...... reactions for bioconjugation.
@en
type
label
Developments and recent advanc ...... reactions for bioconjugation.
@en
prefLabel
Developments and recent advanc ...... reactions for bioconjugation.
@en
P2860
P356
P1476
Developments and recent advanc ...... g reactions for bioconjugation
@en
P2093
Oleksandr Koniev
P2860
P304
P356
10.1039/C5CS00048C
P50
P577
2015-05-22T00:00:00Z