Bulletin of the Chemical Society of Japan · 1993 · 74 citations · 8 references
PharmacyBiochemistryChemistryCarbohydrate ChemistryOrganic ChemistryPolymer ChemistryCarbohydrate CharacterizationCarbohydrate StructureCellulose ChemistryChiral RecognitionChiral Recognition MechanismsStereochemistry Of Sugar Derivatives
Abstract The optical resolving ability of two types of regioselectively carbamoylated cellulose and amylose with 3,5-dimethylphenyl and 3,5-dichlorophenyl isocyanates was evaluated. One had 3,5-dimethylphenylcarbamate groups at the 2 and 3 positions and a 3,5-dichlorophenylcarbamate group at the 6 position; the other had 3,5-dichlorophenylcarbamate groups at the 2 and 3 positions and a 3,5-dimethylphenylcarbamate group at the 6 position. In cellulose derivatives, the side chains at the 2,3, and 6 positions seem to interact complicatedly with racemates. On the other hand, in the amylose derivatives, the side chains at the 2 and 3 positions may mainly influence the chiral recognition ability. The optical resolving abilities of the cellulose and amylose derivatives having irregularly either 3,5-dimethylphenyl- or 3,5-dichlorophenylcarbamate groups at the 2,3, and 6 positions were also examined.
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Yoshio Okamoto, Mitsunobu Kawashima, Koichi Hatada · Journal of Chromatography A · 1986 · 669 citations
Yoshio Okamoto, Mitsunobu Kawashima, Koichi Hatada · Journal of the American Chemical Society · 1984 · 483 citations
Pharmacy, Biochemistry, Chemistry +17