Comparative study on the use of ortho-phthalaldehyde, naphthalene-2,3- dicarboxaldehyde and anthracene-2,3-dicarboxaldehyde reagents for α-amino acids followed by the enantiomer separation of the formed isoindolin-1-one derivatives using quinine-type chiral stationary phases

Journal of Chromatography A

Volumn 1083, Issue 1-2, 2005, Pages 80-88

  Gyimesi Forrás, Krisztina ^a   Leitner, Alexander ^a   Akasaka, Kazuaki ^b   Lindner, Wolfgang ^a  

^a UNIVERSITY OF VIENNA   (Austria)

^b TOHOKU UNIVERSITY   (Japan)

Author keywords

Anthracene 2,3 dicarboxaldehyde; Chiral stationary phases; Enantiomer separation; Isoindolin 1 one; LC; Naphthalene 2,3 dicarboxaldehyde; ortho Phthalaldehyde; Phthalimidine; Quinine carbamate

Indexed keywords

ACETONITRILE; AMINO ACIDS; AROMATIC COMPOUNDS; BINDING ENERGY; DERIVATIVES; DEUTERIUM; LIQUID CHROMATOGRAPHY; MASS SPECTROMETRY; NITROGEN COMPOUNDS; SEPARATION;

ALKALOIDS; CHIRAL STATIONARY PHASES (CSP); ISOINDOLES; ORTHO-PHTHALALDEHYDE (OPA);

ALDEHYDES;

2,3 NAPHTHALENEDICARBOXALDEHYDE; ACETONITRILE; ALDEHYDE DERIVATIVE; ALPHA AMINO ACID; AMINO ACID DERIVATIVE; ANTHRACENE 2,3 DICARBOXALDEHYDE; CINCHONA ALKALOID; ISOINDOLE DERIVATIVE; ISOINDOLIN 1 ONE DERIVATIVE; MERCAPTOETHANOL; MERCAPTOSULFONIC ACID; PHTHALALDEHYDE; SODIUM SULFITE; SULFONIC ACID DERIVATIVE; THIOL DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHIRALITY; DERIVATIZATION; ENANTIOMER; ENANTIOSELECTIVITY; LIQUID CHROMATOGRAPHY; MASS SPECTROMETRY; PRIORITY JOURNAL; STEREOCHEMISTRY;

AMINO ACIDS; ANTHRACENES; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; CINCHONA ALKALOIDS; INDOLES; KINETICS; NAPHTHALENES; O-PHTHALALDEHYDE; PHTHALIMIDES;

CINCHONA; CINCHONA PUBESCENS;

EID: 21544447562     PISSN: 00219673     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.chroma.2005.06.012     Document Type: Article

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