Pattern-based recognition for the rapid determination of identity, concentration, and enantiomeric excess of subtly different threo diols. - Wikidata - awgldk - TriplyDB

Pattern-based recognition for the rapid determination of identity, concentration, and enantiomeric excess of subtly different threo diols.

Pattern-based recognition for the rapid determination of identity, concentration, and enantiomeric excess of subtly different threo diols.

http://www.wikidata.org/entity/Q42584167

about

Decoding complex chemical mixtures with a physical model of a sensor array A general approach to differential sensing using synthetic molecular receptors.Prochelators triggered by hydrogen peroxide provide hexadentate iron coordination to impede oxidative stress Discrimination and classification of ginsenosides and ginsengs using bis-boronic acid receptors in dynamic multicomponent indicator displacement sensor arrays.Array-based detection of persistent organic pollutants via cyclodextrin promoted energy transfer.pH responsive self-healing hydrogels formed by boronate-catechol complexation.Application of a High-Throughput Enantiomeric Excess Optical Assay Involving a Dynamic Covalent Assembly: Parallel Asymmetric Allylation and Ee Sensing of Homoallylic Alcohols.The use of principal component analysis and discriminant analysis in differential sensing routines.Molecular recognition with boronic acids-applications in chemical biology.Chiral donor photoinduced-electron-transfer (d-PET) boronic acid chemosensors for the selective recognition of tartaric acids, disaccharides, and ginsenosides.A cross reactive sensor array to probe divalent metal ions.Fluorescent chirality recognition by simple boronate ensembles with aggregation-induced emission capability.From Substituent Effects to Applications: Enhancing the Optical Response of a Four-Component Assembly for Reporting EE Values.In situ assembly of octahedral Fe(II) complexes for the enantiomeric excess determination of chiral amines using circular dichroism spectroscopy.[(2S,5R)-1-Methyl-5-phenyl-pyrrolidin-2-yl]diphenyl-methanol.A molecular self-assembled colourimetric chemosensor array for simultaneous detection of metal ions in water.The In Situ Enzymatic Screening (ISES) Approach to Reaction Discovery and Catalyst Identification.A convenient fluorescent method to simultaneously determine the enantiomeric composition and concentration of functional chiral amines.Determination of concentration and enantiomeric excess of amines and amino alcohols with a chiral nickel(II) complex.Artificial neural networks for guest chirality classification through supramolecular interactions.Induced helical chirality of perylenebisimide aggregates allows for enantiopurity determination and differentiation of α-hydroxy carboxylates by using circular dichroism.C-hexaphenyl-substituted trianglamine as a chiral solvating agent for carboxylic acids Imine-based chiroptical sensing for analysis of chiral amines: from method design to synthetic application Time–frequency approach in the cluster assignment of amino acids based on their NMR profiles Supramolecular Tandem Enzyme Assays Chiral Recognition by Fluorescence: One Measurement for Two Parameters A Mechanically Controlled Indicator Displacement Assay

P2860

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P2860

Pattern-based recognition for the rapid determination of identity, concentration, and enantiomeric excess of subtly different threo diols.

http://www.wikidata.org/entity/Q42584167

description

2009 nî lūn-bûn

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2009年の論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年论文

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2009年论文

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2009年论文

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name

Pattern-based recognition for ...... subtly different threo diols.

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Pattern-based recognition for ...... subtly different threo diols.

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type

label

Pattern-based recognition for ...... subtly different threo diols.

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Pattern-based recognition for ...... subtly different threo diols.

@nl

prefLabel

Pattern-based recognition for ...... subtly different threo diols.

@en

Pattern-based recognition for ...... subtly different threo diols.

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P1433

Journal of the American Chemical Society

P1476

Pattern-based recognition for ...... subtly different threo diols.

@en

P2093

Eric V Anslyn

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Gabriella M da Cruz

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Leo A Joyce

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Shagufta H Shabbir

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Steven Sorey

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Vincent M Lynch

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P2860

Blue-fluorescent antibodies

Enantioselective fluorescent recognition of a soluble "supported" chiral acid: toward a new method for chiral catalyst screening.

Computational methods for the analysis of chemical sensor array data from volatile analytes.

A colorimetric sensor array for odour visualization.

A structural investigation of the N-B interaction in an o-(N,N-dialkylaminomethyl)arylboronate system.

Double-cuvette ISES: in situ estimation of enantioselectivity and relative rate for catalyst screening.

The sense of smell: multiple olfactory subsystems.

Molecular recognition and self-assembly special feature: A general protocol for creating high-throughput screening assays for reaction yield and enantiomeric excess applied to hydrobenzoin.

Aptamer-based enantioselective competitive binding assay for the trace enantiomer detection.

EMDee: an enzymatic method for determining enantiomeric excess.

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13125-13131

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scholarly article

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10.1021/JA904545D

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36

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131

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26752079

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19691315

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2762347

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