A stereodynamic fluorescent probe for amino acids. Circular dichroism and circularly polarized luminescence analysis.

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Cobalt, nickel, and iron complexes of 8-hydroxyquinoline-di(2-picolyl)amine for light-driven hydrogen evolution.

P2860

Q48293332-0A0A7BAA-ECCE-4744-854B-9FB39E07F031

P2860

A stereodynamic fluorescent probe for amino acids. Circular dichroism and circularly polarized luminescence analysis.

Item

http://www.wikidata.org/entity/Q48360590

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年学术文章

@wuu

2017年学术文章

@zh

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh-hant

name

A stereodynamic fluorescent pr ...... larized luminescence analysis.

@en

A stereodynamic fluorescent pr ...... larized luminescence analysis.

@nl

type

Item

label

A stereodynamic fluorescent pr ...... larized luminescence analysis.

@en

A stereodynamic fluorescent pr ...... larized luminescence analysis.

@nl

prefLabel

A stereodynamic fluorescent pr ...... larized luminescence analysis.

@en

A stereodynamic fluorescent pr ...... larized luminescence analysis.

@nl

P1476

A stereodynamic fluorescent pr ...... olarized luminescence analysis

@en

P2093

Cristiano Zonta

http://www.w3.org/2001/XMLSchema#string

Elena Badetti

http://www.w3.org/2001/XMLSchema#string

Giulia Licini

http://www.w3.org/2001/XMLSchema#string

Nadia Alessandra Carmo Dos Santos

http://www.w3.org/2001/XMLSchema#string

Sergio Abbate

http://www.w3.org/2001/XMLSchema#string

P2860

Mechanisms of tryptophan fluorescence shifts in proteins

Rational design of a fluorescent sensor to simultaneously determine both the enantiomeric composition and the concentration of chiral functional amines.

Dynamic combinatorial libraries: from exploring molecular recognition to systems chemistry.

Intrinsic tryptophan fluorescence in the detection and analysis of proteins: a focus on Förster resonance energy transfer techniques.

A simple method for the determination of enantiomeric excess and identity of chiral carboxylic acids

Dynamic multi-component covalent assembly for the reversible binding of secondary alcohols and chirality sensing

Chiroptical spectra of a series of tetrakis((+)-3-heptafluorobutylyrylcamphorato)lanthanide(III) with an encapsulated alkali metal ion: circularly polarized luminescence and absolute chiral structures for the Eu(III) and Sm(III) complexes

Circularly Polarized Luminescence from Simple Organic Molecules.

Dynamic multicomponent hemiaminal assembly

Application of a High-Throughput Enantiomeric Excess Optical Assay Involving a Dynamic Covalent Assembly: Parallel Asymmetric Allylation and Ee Sensing of Homoallylic Alcohols.

P304

65-73

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1002/CHIR.22780

http://www.w3.org/2001/XMLSchema#string

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Nadia Alessandra Carmo Dos Santos

Elena Badetti

P577

2017-11-04T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

29105860

http://www.w3.org/2001/XMLSchema#string

A stereodynamic fluorescent probe for amino acids. Circular dichroism and circularly polarized luminescence analysis.

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P2860

P2860

A stereodynamic fluorescent probe for amino acids. Circular dichroism and circularly polarized luminescence analysis.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698