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Studies on the chiral recognition of peptide enantiomers by neutral and sulfated β-cyclodextrin and heptakis-(2,3-di-O-acetyl)-β-cyclodextrin using capillary electrophoresis and nuclear magnetic resonance

✍ Scribed by Falko Süß; Claudia Kahle; Ulrike Holzgrabe; Gerhard K. E. Scriba


Publisher
John Wiley and Sons
Year
2002
Tongue
English
Weight
252 KB
Volume
23
Category
Article
ISSN
0173-0835

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Use of heptakis-(2,3-O-dimethyl-6-sulfat
✍ Hong Cai; Gyula Vigh 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 173 KB 👁 1 views

The single isomer, fully and permanently charged heptakis-2,3-di-. methyl-6-sulfato -␤-cyclodextrin was used to study the complexation behavior of the enantiomers of noncharged analytes in capillary electrophoresis. Separation selectivities were calculated from the measured effective mobilities and