Cyclomaltooligosaccharide (cyclodextrin)-assisted enantiomeric recognition of benzo[lmn][3,8]phenanthroline-derived amino acids

Carbohydrate Research

Volumn 340, Issue 7, 2005, Pages 1413-1418

  Jursic, Branko S ^a   Patel, Paresh K ^a  

^a UNIVERSITY OF NEW ORLEANS   (United States)

Author keywords

Cyclodextrin; Cyclomaltooligosaccharide; Electrospray ionization mass spectrometry; Enantiomeric recognition; ESIMS; Molecular aggregation

Indexed keywords

AMINO ACIDS; AROMATIC COMPOUNDS; DERIVATIVES; IONIZATION; MASS SPECTROMETRY; NEGATIVE IONS;

CYCLODEXTRINS; ENANTIOMERIC DISCRIMINATION; NEGATIVE-ION ELECTROSPRAY-IONIZATION MASS SPECTROMETRY (ESIMS); SELF-ASSEMBLY MOLECULAR AGGREGATES;

POLYSACCHARIDES;

AMINO ACID DERIVATIVE; BENZO[LMN][3,8]PHENANTHROLINE; CYCLODEXTRIN DERIVATIVE; PHENANTHROLINE DERIVATIVE; UNCLASSIFIED DRUG;

AQUEOUS SOLUTION; ARTICLE; ELECTROSPRAY MASS SPECTROMETRY; ENANTIOMER; NUCLEAR MAGNETIC RESONANCE; PRIORITY JOURNAL;

EID: 18044386383     PISSN: 00086215     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.carres.2005.03.002     Document Type: Article

References (9)

1. For example, see: C.A. Challener Chiral Drugs 2002 Gower New York
2. H.Y. Aboul-Enein I.W. Wainer The Impact of Stereochemistry on Drug Development and Use 1997 Wiley-Interscience New York
3. Rouhi, A. M. Chem. Eng. News, May 5, 2003, pp 45-55
4. Rouhi, A. M. Chem. Eng. News, May 5, 2003, pp 56-61
5. For more information regarding cyclodextrin complexes, see: H.-J. Schneider, F. Hacket, and V. Rüdiger Chem. Rev. 98 1998 1755 1785
6. M.V. Rekharsky, and Y. Inoue Chem. Rev. 98 1998 1875 1917
7. L. Song, and W.C. Purdy Anal. Chem. 64 1992 1405 1412
8. For the nature of chiral self-assembly see: M.S. Spector, J.V. Selinger, and J.M. Schnur Top. Stereochem. 24 2003 281
9. For some earlier examples of electrospray mass spectroscopic studies of cyclodextrin inclusion complexes see: R. Kobetic, B.S. Jursic, S. Bonnette, J.S.-C. Tsai, and S.J. Salvatore Tetrahedron Lett. 42 2001 6077 and references cited therein