131 related articles for article (PubMed ID: 38408846)
1. Chiral recognition and discrimination studies of tyrosine enantiomers on (-)-18-crown-6-tetracarboxylic acid as a chiral selector by nuclear magnetic resonance spectroscopy and docking simulations.
Lee G; Adhikari S; Lee S; Lee JY; Na YC; Lee W; Bang E
Chirality; 2024 Mar; 36(3):e23656. PubMed ID: 38408846
[TBL] [Abstract][Full Text] [Related]
2. Chiral discrimination studies of (+)-(18-crown-6)-2,3,11,12-tetracarboxylic acid by high-performance liquid chromatography and NMR spectroscopy.
Lee W; Bang E; Baek CS; Lee W
Magn Reson Chem; 2004 Apr; 42(4):389-95. PubMed ID: 15022200
[TBL] [Abstract][Full Text] [Related]
3. Development and application of chiral crown ethers as selectors for chiral separation in high-performance liquid chromatography and nuclear magnetic resonance spectroscopy.
Paik MJ; Kang JS; Huang BS; Carey JR; Lee W
J Chromatogr A; 2013 Jan; 1274():1-5. PubMed ID: 23290338
[TBL] [Abstract][Full Text] [Related]
4. Chiral recognition mechanism studies of Tyr-Arg-Phe-Lys-NH
Upmanis T; Sevostjanovs E; Kažoka H
Chirality; 2024 Jan; 36(1):e23619. PubMed ID: 37700546
[TBL] [Abstract][Full Text] [Related]
5. Noncovalent interactions between ([18]crown-6)-tetracarboxylic acid and amino acids: electrospray-ionization mass spectrometry investigation of the chiral-recognition processes.
Gerbaux P; De Winter J; Cornil D; Ravicini K; Pesesse G; Cornil J; Flammang R
Chemistry; 2008; 14(35):11039-49. PubMed ID: 18956399
[TBL] [Abstract][Full Text] [Related]
6. Stereoisomeric separation of pharmaceutical compounds using CE with a chiral crown ether.
Zhou L; Lin Z; Reamer RA; Mao B; Ge Z
Electrophoresis; 2007 Aug; 28(15):2658-66. PubMed ID: 17657760
[TBL] [Abstract][Full Text] [Related]
7. Chiral NMR discrimination of piperidines and piperazines using (18-crown-6)-2,3,11,12-tetracarboxylic acid.
Lovely AE; Wenzel TJ
J Org Chem; 2006 Nov; 71(24):9178-82. PubMed ID: 17109544
[TBL] [Abstract][Full Text] [Related]
8. 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.
Howard JA; Nonn M; Fulop F; Wenzel TJ
Chirality; 2013 Jan; 25(1):48-53. PubMed ID: 23161804
[TBL] [Abstract][Full Text] [Related]
9. Preparation and evaluation of a chiral stationary phase covalently bound with a chiral pseudo-18-crown-6 ether having a phenolic hydroxy group for enantiomer separation of amino compounds.
Yongzhu J; Hirose K; Nakamura T; Nishioka R; Ueshige T; Tobe Y
J Chromatogr A; 2006 Oct; 1129(2):201-7. PubMed ID: 16872621
[TBL] [Abstract][Full Text] [Related]
10. Nuclear magnetic resonance studies for the chiral recognition of (+)-(R)-18-crown-6-tetracarboxylic acid to amino compounds.
Machida Y; Kagawa M; Nishi H
J Pharm Biomed Anal; 2003 Jan; 30(6):1929-42. PubMed ID: 12485736
[TBL] [Abstract][Full Text] [Related]
11. Utilization of (18-crown-6)-2,3,11,12-tetracarboxylic acid as a chiral NMR solvating agent for diamines and β-amino acids.
Rodriguez YC; Duarte TM; Szakonyi Z; Forró E; Fülöp F; Wenzel TJ
Chirality; 2015 Oct; 27(10):708-15. PubMed ID: 26285042
[TBL] [Abstract][Full Text] [Related]
12. Chiral recognition of peptide enantiomers by cinchona alkaloid derived chiral selectors: mechanistic investigations by liquid chromatography, NMR spectroscopy, and molecular modeling.
Czerwenka C; Zhang MM; Kählig H; Maier NM; Lipkowitz KB; Lindner W
J Org Chem; 2003 Oct; 68(22):8315-27. PubMed ID: 14575453
[TBL] [Abstract][Full Text] [Related]
13. Enantiomeric resolution of quinolones on crown ether CSP: Thermodynamics, chiral discrimination mechanism and application in biological samples.
ALOthman ZA; Badjah AY; Alsheetan KM; Suhail M; Ali I
J Chromatogr B Analyt Technol Biomed Life Sci; 2021 Mar; 1166():122550. PubMed ID: 33545563
[TBL] [Abstract][Full Text] [Related]
14. Development of HPLC Chiral Stationary Phases Based on (+)-(18-Crown-6)-2,3,11,12-tetracarboxylic Acid and Their Applications.
Hyun MH
Chirality; 2015 Sep; 27(9):576-88. PubMed ID: 26237013
[TBL] [Abstract][Full Text] [Related]
15. Preparation of Two New Diasteromeric Chiral Stationary Phases Based on (+)-(18-Crown-6)-2,3,11,12-tetracarboxylic Acid and (R)- or (S)-1-(1-Naphthyl)ethylamine and Chiral Tethering Group Effect on the Chiral Recognition.
Agneeswari R; Sung JY; Jo ES; Jeon HY; Tamilavan V; Hyun MH
Molecules; 2016 Aug; 21(8):. PubMed ID: 27529205
[TBL] [Abstract][Full Text] [Related]
16. HPLC enantioseparation of beta2-homoamino acids using crown ether-based chiral stationary phase.
Berkecz R; Ilisz I; Misicka A; Tymecka D; Fülöp F; Choi HJ; Hyun MH; Péter A
J Sep Sci; 2009 Apr; 32(7):981-7. PubMed ID: 19306252
[TBL] [Abstract][Full Text] [Related]
17. Enantiomeric discrimination of chiral organic salts by chiral aza-15-crown-5 ether with C 1 symmetry: experimental and theoretical approaches.
Kocakaya SÖ; Turgut Y; Pirinççioglu N
J Mol Model; 2015 Mar; 21(3):55. PubMed ID: 25701087
[TBL] [Abstract][Full Text] [Related]
18. Chiral recognition of amino acid enantiomers by a crown ether: chiroptical IR-VCD response and computational study.
Avilés-Moreno JR; Quesada-Moreno MM; López-González JJ; Martínez-Haya B
J Phys Chem B; 2013 Aug; 117(32):9362-70. PubMed ID: 23848404
[TBL] [Abstract][Full Text] [Related]
19. Influence of amino acid residue on chromatographic behaviour of μ-opioid receptor agonist tetrapeptide analogue on crown ether based chiral stationary phase.
Upmanis T; Kažoka H
J Chromatogr A; 2022 Jun; 1673():463059. PubMed ID: 35487117
[TBL] [Abstract][Full Text] [Related]
20. High-performance liquid chromatographic enantioseparation of beta-amino acid stereoisomers on a (+)-(18-crown-6)-2,3,11,12-tetracarboxylic acid-based chiral stationary phase.
Berkecz R; Sztojkov-Ivanov A; Ilisz I; Forró E; Fülöp F; Hyun MH; Péter A
J Chromatogr A; 2006 Aug; 1125(1):138-43. PubMed ID: 16843474
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
