Assignment of the absolute configuration of polyfunctional compounds by NMR using chiral derivatizing agents.
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Involucratusins A-H: Unusual Cadinane Dimers from Stahlianthus involucratus with Multidrug Resistance Reversal ActivitySynthesis and Utilization of Trialkylammonium-Substituted Cyclodextrins as Water-Soluble Chiral NMR Solvating Agents for Anionic Compounds.Highly enantioselective synthesis of γ-, δ-, and ε-chiral 1-alkanols via Zr-catalyzed asymmetric carboalumination of alkenes (ZACA)-Cu- or Pd-catalyzed cross-coupling.A new diphenyl ether derivative from Mirabilis himalaica.The determination of the absolute configuration of a chiral 2,3'-diindolylarylmethane by NMR spectroscopy.Recent Advances in Multinuclear NMR Spectroscopy for Chiral Recognition of Organic Compounds.Design of Selenium-Based Chiral Chemical Probes for Simultaneous Enantio- and Chemosensing of Chiral Carboxylic Acids with Remote Stereogenic Centers by NMR Spectroscopy.Stereochemistry of the Brivaracetam Diastereoisomers.Improving the performance of J-modulated ADEQUATE experiments through homonuclear decoupling and non-uniform sampling.Determination of the absolute stereostructure of a cyclic azobenzene from the crystal structure of the precursor containing a heavy element.Structure and biosynthetic assembly of gulmirecins, macrolide antibiotics from the predatory bacterium Pyxidicoccus fallax.Application of NMR spectroscopy for assignment of the absolute configuration of 8-tert-butyl-2-hydroxy-7-methoxy-8-methyl-9-oxa-6-azaspiro[4.5]dec-6-en-10-one.Cooperative use of VCD and XRD for the determination of tetrahydrobenzoisoquinolines absolute configuration: a reliable proof of memory of chirality and retention of configuration in enediyne rearrangements.Utilization of (18-crown-6)-2,3,11,12-tetracarboxylic acid as a chiral NMR solvating agent for diamines and β-amino acids.Multiple homonuclear band-selective decoupling NMR: Fast and unambiguous determination of diastereomeric excess.Host-Guest Assembly of a Molecular Reporter with Chiral Cyanohydrins for Assignment of Absolute Stereochemistry.The assignment of the configuration for α-hydroxy acid esters using a CEC strategy.Characteristic conformation of Mosher's amide elucidated using the cambridge structural database.The first fluorogenic sensor for sphingosine-1-phosphate lyase activity in intact cells.Enantiopure O-ethyl phenylphosphonothioic acid: a solvating agent for the determination of enantiomeric excesses.Nodulisporipyrones A-D, new bioactive α-pyrone derivatives from Nodulisporium sp.
P2860
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P2860
Assignment of the absolute configuration of polyfunctional compounds by NMR using chiral derivatizing agents.
description
2012 nî lūn-bûn
@nan
2012 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
Assignment of the absolute con ...... ng chiral derivatizing agents.
@ast
Assignment of the absolute con ...... ng chiral derivatizing agents.
@en
Assignment of the absolute con ...... ng chiral derivatizing agents.
@nl
type
label
Assignment of the absolute con ...... ng chiral derivatizing agents.
@ast
Assignment of the absolute con ...... ng chiral derivatizing agents.
@en
Assignment of the absolute con ...... ng chiral derivatizing agents.
@nl
prefLabel
Assignment of the absolute con ...... ng chiral derivatizing agents.
@ast
Assignment of the absolute con ...... ng chiral derivatizing agents.
@en
Assignment of the absolute con ...... ng chiral derivatizing agents.
@nl
P356
P1433
P1476
Assignment of the absolute con ...... ng chiral derivatizing agents.
@en
P2093
P304
P356
10.1021/CR2003344
P577
2012-06-01T00:00:00Z