𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Chiral resolution of flurbiprofen and ketoprofen enantiomers by HPLC on a glycopeptide-type column chiral stationary phase

✍ Scribed by F. Péhourcq; C. Jarry; B. Bannwarth

Publisher
John Wiley and Sons
Year
2001
Tongue
English
Weight
84 KB
Volume
15
Category
Article
ISSN
0269-3879

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Chiral recognition mechanism for the res
Chiral recognition mechanism for the resolution of enantiomers on a highly effective HPLC chiral stationary phase derived from (R)-4-hydroxyphenylglycine
✍ Myung Ho Hyun; Chung-Sik Min 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 191 KB 👁 2 views

A chiral stationary phase (CSP 1) prepared starting from (R)-4hydroxyphenylglycine and then grafting (R)-N-butanoyl-4-allyloxyphenylglycine Npropyl amide to silica gel was found to be very effective in separating the enantiomers of N-(3,5-dinitrobenzoyl)-␣-amino amides. From the chromatographic beha

Resolution of some 4-benzofurazanyl and
Resolution of some 4-benzofurazanyl and 4-benzofuroxanyl 1,4-dihydropyridine derivatives by chiral HPLC on Whelk-o1 and some polysaccharide chiral stationary phases
✍ Sonja Visentin; Pascale Amiel; Alberto Gasco; Brice Bonnet; Cristina Suteu; Chri 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 118 KB

The chromatographic chiral resolution of racemic methyl 1, 4-dihydro-2,6-dimethyl-5-nitro-4-benzofurazanyl-3-carboxylates 1 and 2 and their benzofuroxanyl analogues 3 and 4 were studied on Whelk-O1, Chiralcel OD-H, Chiralcel OJ, and Chiralpak AD and AS. These CSPs were selected on the basis of the r

HPLC enantioseparation on cellulose tris
HPLC enantioseparation on cellulose tris(3,5-dimethylphenylcarbamate) as a chiral stationary phase: Influences of pore size of silica gel, coating amount, coating solvent, and column temperature on chiral discrimination
✍ Eiji Yashima; Pennapa Sahavattanapong; Yoshio Okamoto 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 444 KB 👁 2 views

Cellulose tris(3,5dimethylphenylcarbamate) (CDMPC) was coated on largepore silica gels and used as a chiral stationary phase (CSP) for high-performance liquid chromatographic separation of enantiomers. The influences of pore size of silica gel, coating amount of CDMPC, coating solvent, and column te

Diphenylethanediamine (DPEDA) as chiral
Diphenylethanediamine (DPEDA) as chiral selector: VII. Efficient HPLC resolution of a series of underivatized diarylcarbinols on a chiral stationary phase based on C5-amide-bonded N-3,5-dinitrobenzoyl-DPEDA
✍ Norbert M. Maier; Georg Uray 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 335 KB 👁 1 views

Fast and efficient baseline separation of asymmetrically substituted diarylmethanols and 1,ldiarylethanols was achieved on an endcapped, amidelinked N-3,Minitrobenzoylated, (R,R)-1,2diphenyl-l,2-ethanediaminederived chiral stationary phase (CSP) . Optimal enantioselectivities on this CSP were obtain