Metal-free triazole formation as a tool for bioconjugation.
about
Thiol-selective fluorogenic probes for labeling and release.Cu-free click cycloaddition reactions in chemical biologyBioorthogonal chemistry: fishing for selectivity in a sea of functionalitySelective labeling of living cells by a photo-triggered click reactionClick chemistry in complex mixtures: bioorthogonal bioconjugation(E,E)-1,5-Cyclooctadiene: a small and fast click-chemistry multitalentAqueous-phase deactivation and intramolecular [2 + 2 + 2] cycloaddition of oxanorbornadiene estersBioorthogonal chemistry: recent progress and future directions.Synthesis of a DOTA--biotin conjugate for radionuclide chelation via Cu-free click chemistry.Degradable conjugates from oxanorbornadiene reagentsA Mild, Large-Scale Synthesis of 1,3-Cyclooctanedione: Expanding Access to Difluorinated Cyclooctyne for Copper-Free Click Chemistry.Bringing chemistry to life.Peptidylation for the determination of low-molecular-weight compounds by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.A Synthetic Toolbox for the In Situ Formation of Functionalized Homo- and Heteropolysaccharide-Based Hydrogel Libraries.Imaging beyond the proteomeSecond-generation difluorinated cyclooctynes for copper-free click chemistry.1,3-Dipolar Cycloaddition with Diazo Groups: Noncovalent Interactions Overwhelm Strain.Polypeptide-polymer bioconjugates.Staudinger ligation as a method for bioconjugation.Synthetic strategies for the biotinylation of bioactive small molecules.Bioorthogonal chemistry for pre-targeted molecular imaging--progress and prospects.Bioorthogonal labelling of biomolecules: new functional handles and ligation methods.Smart chemistry in polymeric nanomedicine."Click" reactions: a versatile toolbox for the synthesis of peptide-conjugates.Orthogonality in organic, polymer, and supramolecular chemistry: from Merrifield to click chemistry.Selective chemical labeling of proteins.From "Click" to "Fenton" chemistry for 5-bromo-2'-deoxyuridine determination.Visualizing metabolically labeled glycoconjugates of living cells by copper-free and fast huisgen cycloadditions.Synthesis of Magnetic-Nanoparticle/Ansamitocin Conjugates-Inductive Heating Leads to Decreased Cell Proliferation In Vitro and Attenuation Of Tumour Growth In Vivo.Towards a biocompatible artificial lung: Covalent functionalization of poly(4-methylpent-1-ene) (TPX) with cRGD pentapeptide.Fine-Tuning Strain and Electronic Activation of Strain-Promoted 1,3-Dipolar Cycloadditions with Endocyclic Sulfamates in SNO-OCTsBioorthogonal fluorescent labeling of functional G-protein-coupled receptors.Norbornenes in inverse electron-demand Diels-Alder reactions.Efficient cyanoaromatic photosensitizers for singlet oxygen production: synthesis and characterization of the transient reactive species.Stabilized Wittig olefination for bioconjugation.Chemical Functionalization of Polysaccharides-Towards Biocompatible Hydrogels for Biomedical Applications.Catalyst-free room-temperature iClick reaction of molybdenum(ii) and tungsten(ii) azide complexes with electron-poor alkynes: structural preferences and kinetic studies.Assessing the whole range of CuAAC mechanisms by DFT calculations--on the intermediacy of copper acetylides.Metal-Free Poly-Cycloaddition of Activated Azide and Alkynes toward Multifunctional Polytriazoles: Aggregation-Induced Emission, Explosive Detection, Fluorescent Patterning, and Light Refraction.A fast, visible-light-sensitive azobenzene for bioorthogonal ligation.
P2860
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P2860
Metal-free triazole formation as a tool for bioconjugation.
description
2007 nî lūn-bûn
@nan
2007 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Metal-free triazole formation as a tool for bioconjugation.
@ast
Metal-free triazole formation as a tool for bioconjugation.
@en
Metal-free triazole formation as a tool for bioconjugation.
@nl
type
label
Metal-free triazole formation as a tool for bioconjugation.
@ast
Metal-free triazole formation as a tool for bioconjugation.
@en
Metal-free triazole formation as a tool for bioconjugation.
@nl
prefLabel
Metal-free triazole formation as a tool for bioconjugation.
@ast
Metal-free triazole formation as a tool for bioconjugation.
@en
Metal-free triazole formation as a tool for bioconjugation.
@nl
P2093
P356
P1433
P1476
Metal-free triazole formation as a tool for bioconjugation.
@en
P2093
A Ton J Dirks
Floris L van Delft
Floris P J T Rutjes
Jeroen J L M Cornelissen
Marjoke F Debets
Roeland J M Nolte
Sander S van Berkel
P304
P356
10.1002/CBIC.200700278
P577
2007-09-01T00:00:00Z