A detailed examination of boronic acid–diol complexation
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Nanostructures for the Inhibition of Viral InfectionsResponsive Boronic Acid-Decorated (Co)polymers: From Glucose Sensors to Autonomous Drug DeliveryOrganocatalytic Conversion of Cellulose into a Platform ChemicalNon inflammatory boronate based glucose-responsive insulin delivery systemsUltrafast NMR T1 relaxation measurements: probing molecular properties in real timeInteraction of green tea polyphenol epigallocatechin-3-gallate with sunitinib: potential risk of diminished sunitinib bioavailabilityFlexible three-dimensional electrochemical glucose sensor with improved sensitivity realized in hybrid polymer microelectromechanical systems techniqueStructures of carbohydrate-boronic acid complexes determined by NMR and molecular modelling in aqueous alkaline media.Discovery of a novel activator of KCNQ1-KCNE1 K channel complexes.Design, synthesis, and screening of a library of peptidyl bis(boroxoles) as oligosaccharide receptors in water: identification of a receptor for the tumor marker TF-antigen disaccharide.Chemoselective oxidation of aryl organoboron systems enabled by boronic acid-selective phase transferDynamic combinatorial chemistry employing boronic acids/boronate esters leads to potent oxygenase inhibitors.Schiff base formation and recognition of amino sugars, aminoglycosides and biological polyamines by 2-formyl phenylboronic acid in aqueous solution.Reversible click reactions with boronic acids to build supramolecular architectures in water.Phenylboronate chromatography selectively separates glycoproteins through the manipulation of electrostatic, charge transfer, and cis-diol interactions.Preclinical evaluation of the antitumor activity of bortezomib in combination with vitamin C or with epigallocatechin gallate, a component of green tea.Development of phenylboronic acid-functionalized nanoparticles for emodin delivery.Reversible linkage of two distinct small molecule inhibitors of Myc generates a dimeric inhibitor with improved potency that is active in myc over-expressing cancer cell lines.pH responsive self-healing hydrogels formed by boronate-catechol complexation.Addition of Phenylboronic Acid to Malus domestica Pollen Tubes Alters Calcium Dynamics, Disrupts Actin Filaments and Affects Cell Wall Architecture.Monosaccharides as Versatile Units for Water-Soluble Supramolecular Polymers.Discrimination of Saccharides by a Simple Array.Self-assembly of peptide boroxoles on cis-dihydroxylated oligoamide templates in water.pH-Triggered reversible morphological inversion of orthogonally-addressable poly(3-acrylamidophenylboronic acid)-block-poly(acrylamidoethylamine) micelles and their shell crosslinked nanoparticles.Phenylboronic acid-functionalized magnetic nanoparticles for one-step saccharides enrichment and mass spectrometry analysisA Novel Quantitative Mass Spectrometry Platform for Determining Protein O-GlcNAcylation Dynamics.In situ recognition of cell-surface glycans and targeted imaging of cancer cellsA Nonoxidative Electrochemical Sensor Based on a Self-Doped Polyaniline/Carbon Nanotube Composite for Sensitive and Selective Detection of the Neurotransmitter Dopamine: A Review.Boron-containing inhibitors of synthetases.Adverse effects of concentrated green tea extracts.Chemical methods for degradation of target oligosaccharides using designed light-activatable organic molecules.Is boron a prebiotic element? A mini-review of the essentiality of boron for the appearance of life on earth.The development of boronic acids as sensors and separation tools.Applications of reversible covalent chemistry in analytical sample preparation.Towards smart tattoos: implantable biosensors for continuous glucose monitoring.Chemical biology based on target-selective degradation of proteins and carbohydrates using light-activatable organic molecules.Binding sugars: from natural lectins to synthetic receptors and engineered neolectins.Responsive materials for self-regulated insulin delivery.Boronic acid-containing hydrogels: synthesis and their applications.Interaction modes and approaches to glycopeptide and glycoprotein enrichment.
P2860
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P2860
A detailed examination of boronic acid–diol complexation
description
im Juni 2002 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
@nl
наукова стаття, опублікована в червні 2002
@uk
name
A detailed examination of boronic acid–diol complexation
@en
A detailed examination of boronic acid–diol complexation
@nl
type
label
A detailed examination of boronic acid–diol complexation
@en
A detailed examination of boronic acid–diol complexation
@nl
prefLabel
A detailed examination of boronic acid–diol complexation
@en
A detailed examination of boronic acid–diol complexation
@nl
P1433
P1476
A detailed examination of boronic acid–diol complexation
@en
P2093
Binghe Wang
Greg Springsteen
P304
P356
10.1016/S0040-4020(02)00489-1
P577
2002-06-01T00:00:00Z