Organic azides: an exploding diversity of a unique class of compounds.
about
Synthesis of coumarin or ferrocene labeled nucleosides via Staudinger ligationVegetable oil derived solvent, and catalyst free "click chemistry" thermoplastic polytriazolesAzidation in the Difunctionalization of OlefinsSynthesis and Chemistry of Organic Geminal Di- and TriazidesSix-Membered Aromatic Polyazides: Synthesis and ApplicationAdvances in BioconjugationOne-step (18)F labeling of biomolecules using organotrifluoroboratesCYP450 Enzymes Effect Oxygen-Dependent Reduction of Azide-Based Fluorogenic DyesMechanistic Insights into the H₂S-Mediated Reduction of Aryl Azides Commonly Used in H₂S DetectionFluorogenic label for biomolecular imaging.Synthesis and promising properties of a new family of high-nitrogen compounds: polyazido- and polyamino-substituted N,N'-azo-1,2,4-triazoles.Staudinger ligation towards cyclodextrin dimers in aqueous/organic media. Synthesis, conformations and guest-encapsulation ability.Reactivity of intein thioesters: appending a functional group to a protein.Difluorophosphoryl nitrene F2P(O)N: matrix isolation and unexpected rearrangement to F2PNO.Coulombic effects on the traceless Staudinger ligation in water.Janus-type dendrimer-like poly(ethylene oxide)sTyrosine-sulfate isosteres of CCR5 N-terminus as tools for studying HIV-1 entry.Product-Derived Bimetallic Palladium Complex Catalyzes Direct Carbonylation of Sulfonylazides.A multicomponent CuAAC "click" approach to a library of hybrid polydentate 2-pyridyl-1,2,3-triazole ligands: new building blocks for the generation of metallosupramolecular architectures.Water-soluble phosphinothiols for traceless staudinger ligation and integration with expressed protein ligation.Intramolecular Fe(II)-catalyzed N-O or N-N bond formation from aryl azidesSynthesis of 1,2,4-triazines and the triazinoisoquinolinedione DEF ring system of noelaquinone.4-Des-oxy-4β-(4-methoxy-carbonyl-1,2,3-triazol-1-yl)podophyllotoxin dichloro-methane solvate.Use of propidium monoazide and increased amplicon length reduce false-positive signals in quantitative PCR for bioburden analysis.A two-directional strategy for the diversity-oriented synthesis of macrocyclic scaffolds.New methodologies in the construction of dendritic materials.Recent advances in transition metal-catalyzed N-atom transfer reactions of azidesReversible hydrazide chemistry-based enrichment for O-GlcNAc-modified peptides and glycopeptides having non-reducing GlcNAc residues.Metal-catalysed azidation of tertiary C-H bonds suitable for late-stage functionalizationA Versatile Monomer for Preparing Well-Defined Functional Polycarbonates and Poly(ester-carbonates)1,3-Dipolar cycloaddition reactivities of perfluorinated aryl azides with enamines and strained dipolarophilesReactivities of vinyl azides and their recent applications in nitrogen heterocycle synthesis.Diazo groups endure metabolism and enable chemoselectivity in cellulo.Carbohydrate conjugation through microwave-assisted functionalization of single-walled carbon nanotubes using perfluorophenyl azides.Design of a papain immobilized antimicrobial food package with curcumin as a crosslinker.Decomposition of fluorophosphoryl diazide: a joint experimental and theoretical study.Preparation of azidoaryl- and azidoalkyloxazoles for click chemistry.Temperature dependence of turnover in a Sc(OTf)3-catalyzed intramolecular Schmidt reaction.Fast dye salts provide fast access to azidoarene synthons in multi-step one-pot tandem click transformationsIntramolecular and Intermolecular Schmidt Reactions of Alkyl Azides with Aldehydes.
P2860
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P2860
Organic azides: an exploding diversity of a unique class of compounds.
description
2005 nî lūn-bûn
@nan
2005 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Organic azides: an exploding diversity of a unique class of compounds.
@ast
Organic azides: an exploding diversity of a unique class of compounds.
@en
Organic azides: an exploding diversity of a unique class of compounds.
@nl
type
label
Organic azides: an exploding diversity of a unique class of compounds.
@ast
Organic azides: an exploding diversity of a unique class of compounds.
@en
Organic azides: an exploding diversity of a unique class of compounds.
@nl
prefLabel
Organic azides: an exploding diversity of a unique class of compounds.
@ast
Organic azides: an exploding diversity of a unique class of compounds.
@en
Organic azides: an exploding diversity of a unique class of compounds.
@nl
P2093
P356
P1476
Organic azides: an exploding diversity of a unique class of compounds.
@en
P2093
Kerstin Knepper
Stefan Bräse
Viktor Zimmermann
P304
P356
10.1002/ANIE.200400657
P407
P50
P577
2005-08-01T00:00:00Z