Synthesis of a single-isomer sulfated beta-cyclodextrin carrying nonidentical substituents at all of the C2, C3, and C6 positions and its use for the electrophoretic separation of enantiomers in acidic aqueous and methanolic background electrolytes. Part 2: Heptakis(2-O-methyl-6-O-sulfo) cyclomaltoheptaose.
Busby, M Brent
Synthesis of a single-isomer sulfated beta-cyclodextrin carrying nonidentical substituents at all of the C2, C3, and C6 positions and its use for the electrophoretic separation of enantiomers in acidic aqueous and methanolic background electrolytes. Part 2: Heptakis(2-O-methyl-6-O-sulfo) cyclomaltoheptaose. [electronic resource] - Electrophoresis Oct 2005 - 3849-60 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
0173-0835
10.1002/elps.200500191 doi
Electrophoresis, Capillary--methods
Hydrogen-Ion Concentration
Methanol
Solvents
Stereoisomerism
Sulfates
beta-Cyclodextrins--chemical synthesis
Synthesis of a single-isomer sulfated beta-cyclodextrin carrying nonidentical substituents at all of the C2, C3, and C6 positions and its use for the electrophoretic separation of enantiomers in acidic aqueous and methanolic background electrolytes. Part 2: Heptakis(2-O-methyl-6-O-sulfo) cyclomaltoheptaose. [electronic resource] - Electrophoresis Oct 2005 - 3849-60 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
0173-0835
10.1002/elps.200500191 doi
Electrophoresis, Capillary--methods
Hydrogen-Ion Concentration
Methanol
Solvents
Stereoisomerism
Sulfates
beta-Cyclodextrins--chemical synthesis