Chiral recognition ability and solvent versatility of bonded amylose tris-(3,5-dimethylphenylcarbamate) chiral stationary phase: enantioselective liquid chromatographic resolution of racemic N-alkylated barbiturates and thalidomide analogs

Ashraf Ghanem; Ebtessam Al-Humaidi

Chiral recognition ability and solvent versatility of bonded amylose tris-(3,5-dimethylphenylcarbamate) chiral stationary phase: enantioselective liquid chromatographic resolution of racemic N-alkylated barbiturates and thalidomide analogs

Ashraf Ghanem
, Ebtessam Al-Humaidi

Research output: Contribution to journal › Article › peer-review

Original language	English
Pages (from-to)	477-484
Number of pages	8
Journal	Chirality
Volume	19
Issue number	6
Publication status	Published - 2007

Cite this

@article{2758bd225e8f4afca648a5662b510296,

title = "Chiral recognition ability and solvent versatility of bonded amylose tris-(3,5-dimethylphenylcarbamate) chiral stationary phase: enantioselective liquid chromatographic resolution of racemic N-alkylated barbiturates and thalidomide analogs",

author = "Ashraf Ghanem and Ebtessam Al-Humaidi",

year = "2007",

language = "English",

volume = "19",

pages = "477--484",

journal = "Chirality",

issn = "0899-0042",

publisher = "Wiley-Liss Inc.",

number = "6",

}

Chiral recognition ability and solvent versatility of bonded amylose tris-(3,5-dimethylphenylcarbamate) chiral stationary phase: enantioselective liquid chromatographic resolution of racemic N-alkylated barbiturates and thalidomide analogs. / Ghanem, Ashraf; Al-Humaidi, Ebtessam.
In: Chirality, Vol. 19, No. 6, 2007, p. 477-484.

Research output: Contribution to journal › Article › peer-review

TY - JOUR

T1 - Chiral recognition ability and solvent versatility of bonded amylose tris-(3,5-dimethylphenylcarbamate) chiral stationary phase: enantioselective liquid chromatographic resolution of racemic N-alkylated barbiturates and thalidomide analogs

AU - Ghanem, Ashraf

AU - Al-Humaidi, Ebtessam

PY - 2007

Y1 - 2007

M3 - Article

SN - 0899-0042

VL - 19

SP - 477

EP - 484

JO - Chirality

JF - Chirality

IS - 6

ER -