Chiral separation of amino acids by chiral octamide derivatives of calixarenes derived from resorcinol by impregnation on a polymeric support

Seyhan, SERAP; Ozbayrak, O; Demirel, N; MERDİVAN, MELEK; Pirinccioglu, N

doi:10.1016/j.tetasy.2005.10.012

Chiral separation of amino acids by chiral octamide derivatives of calixarenes derived from resorcinol by impregnation on a polymeric support

Atıf İçin Kopyala

Seyhan S., Ozbayrak O., Demirel N., MERDİVAN M., Pirinccioglu N.

TETRAHEDRON-ASYMMETRY, cilt.16, sa.22, ss.3735-3738, 2005 (SCI-Expanded)

Yayın Türü: Makale / Tam Makale
Cilt numarası: 16 Sayı: 22
Basım Tarihi: 2005
Doi Numarası: 10.1016/j.tetasy.2005.10.012
Dergi Adı: TETRAHEDRON-ASYMMETRY
Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
Sayfa Sayıları: ss.3735-3738
Dokuz Eylül Üniversitesi Adresli: Evet

Özet

Chiral amide derivatives of octaester calixresorcarene were synthesized and employed as chiral stationary phases for chiral discrimination of amino acid derivatives. Enantiomers of phenylglycine and tryptophan were easily discriminated as their sodium and potassium salts. In addition, phenylalanine-trytophan, phenylglycine-trytophan mixtures were separated by column chromatography. (c) 2005 Elsevier Ltd. All rights reserved.