Comparative evaluation of the chiral recognition potential of single-isomer sulfated beta-cyclodextrin synthesis intermediates in non-aqueous capillary electrophoresis-Reference-Cited by-同舟云学术

Comparative evaluation of the chiral recognition potential of single-isomer sulfated beta-cyclodextrin synthesis intermediates in non-aqueous capillary electrophoresis

Published:2016-10 Issue: Volume:1467 Page:454-462
ISSN:0021-9673
Container-title:Journal of Chromatography A
language:en
Short-container-title:Journal of Chromatography A

Author:

Fejős Ida,Varga Erzsébet,Benkovics Gábor,Darcsi András,Malanga Milo,Fenyvesi Éva,Sohajda Tamás,Szente Lajos,Béni Szabolcs^ORCID

Funder

OTKA PD

the Marie Curie Programme Initial Training Network

Publisher

Elsevier BV

Subject

Organic Chemistry,General Medicine,Biochemistry,Analytical Chemistry

Reference44 articles.

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3. Synthesis of heptakis(2-O-methyl-3-O-acetyl-6-O-sulfo)-cyclomaltoheptaose, a single-isomer, sulfated β-cyclodextrin carrying nonidentical substitutents at all the C2, C3, and C6 positions and its use for the capillary electrophoretic separation of enantiomers in acidic aqueous and methanolic background electrolytes

4. Capillary electrophoretic separation of weak base enantiomers using the single-isomer heptakis-(2, 3-dimethyl-6-sulfato)-β-cyclodextrin as resolving agent and methanol as background electrolyte solvent;Cai;J. Pharm. Biomed. Anal.,1998

5. Capillary electrophoretic separation of enantiomers using the single isomer heptakis-(2,3-dimethyl-6-sulfato)-β-cyclodextrin as chiral resolving agent in methanol-water background electrolytes;Cai;J. Chromatogr. A,1998

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