1989
DOI: 10.1007/bf02321273
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New chiral derivatization reagent for the resolution of amino acids as diastereomers by TLC and HPLC

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Cited by 17 publications
(2 citation statements)
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“…LOD of the minor enantiomer at S/N =3 was 0.1% [6]. -NSPC was useful for the separation of 18 DL-amino acids by TLC and adsorption HPLC with a Zorbax Sil column (4.6 mm ID x 15 cm) [7].…”
Section: Enantiomer Separation Of Pharmaceuticals By Hplc and Its Appmentioning
confidence: 99%
“…LOD of the minor enantiomer at S/N =3 was 0.1% [6]. -NSPC was useful for the separation of 18 DL-amino acids by TLC and adsorption HPLC with a Zorbax Sil column (4.6 mm ID x 15 cm) [7].…”
Section: Enantiomer Separation Of Pharmaceuticals By Hplc and Its Appmentioning
confidence: 99%
“…A new chiral reagent, NSP-C1, was synthesized and used to derivatize amino acid diastereomers, and the resulting amides were resolved by TLC (114). TLC on Chiralplates with acetonitrile-methanol-water (4:1:1) mobile phase was used to evaluate reaction products in the synthesis of modified phenylalanine and tyrosine derivatives and for the determination of the amino acid configuration of synthetic peptide analogues prepared starting from the racemic aromatic amino acids (115).…”
Section: Applicationsmentioning
confidence: 99%