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description
| - wetenschappelijk artikel (nl)
- wüsseschaftlicher Artikel, wo im März 2000 veröffentlicht worden isch (gsw)
- im März 2000 veröffentlichter wissenschaftlicher Artikel (de)
- наукова стаття, опублікована в березні 2000 (uk)
- artículu científicu espublizáu en marzu de 2000 (ast)
- scientific article published on 01 March 2000 (en)
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rdfs:label
| - (+)-(18-Crown-6)-2,3,11,12-tetracarboxylic acid and its Ytterbium(III) complex as chiral NMR discriminating agents (en)
- (+)-(18-Crown-6)-2,3,11,12-tetracarboxylic acid and its Ytterbium(III) complex as chiral NMR discriminating agents (nl)
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skos:prefLabel
| - (+)-(18-Crown-6)-2,3,11,12-tetracarboxylic acid and its Ytterbium(III) complex as chiral NMR discriminating agents (en)
- (+)-(18-Crown-6)-2,3,11,12-tetracarboxylic acid and its Ytterbium(III) complex as chiral NMR discriminating agents (nl)
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name
| - (+)-(18-Crown-6)-2,3,11,12-tetracarboxylic acid and its Ytterbium(III) complex as chiral NMR discriminating agents (en)
- (+)-(18-Crown-6)-2,3,11,12-tetracarboxylic acid and its Ytterbium(III) complex as chiral NMR discriminating agents (nl)
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title
| - (+)-(18-Crown-6)-2,3,11,12-tetracarboxylic acid and its Ytterbium(III) complex as chiral NMR discriminating agents (en)
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is about
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is cites work
of | - Calix[4]arene, calix[4]resorcarene, and cyclodextrin derivatives and their lanthanide complexes as chiral NMR shift reagents
- Water-soluble calix[4]resorcinarenes as chiral NMR solvating agents for bicyclic aromatic compounds
- Nuclear magnetic resonance studies for the chiral recognition of (+)-(R)-18-crown-6-tetracarboxylic acid to amino compounds
- Chiral NMR discrimination of amines: analysis of secondary, tertiary, and prochiral amines using (18-crown-6)-2,3,11,12-tetracarboxylic acid
- Chiral reagents for the determination of enantiomeric excess and absolute configuration using NMR spectroscopy
- Synthesis, LSD1 Inhibitory Activity, and LSD1 Binding Model of Optically Pure Lysine-PCPA Conjugates
- Utilization of (18-crown-6)-2,3,11,12-tetracarboxylic acid as a chiral NMR solvating agent for diamines and β-amino acids
- Enantiomeric discrimination of isoxazoline fused β-amino acid derivatives using (18-crown-6)-2,3,11,12-tetracarboxylic acid as a chiral NMR solvating agent
- Chiral recognition of ethers by NMR spectroscopy
- Application of L-proline derivatives as chiral shift reagents for enantiomeric recognition of carboxylic acids.
- Discrimination of enantiomers of alpha-amino acids by chiral derivatizing reagents from trans-1,2-diaminocyclohexane
- Guest-dependent conformation of 18-crown-6 tetracarboxylic acid: relation to chiral separation of racemic amino acids
- Enantiomeric NMR signal separation behavior and mechanism of samarium(III) and neodymium(III) complexes with (S,S)-ethylenediamine-N,N'-disuccinate.
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