Synthesis and Inclusion Ability of New Cyclodextrin Analogues Incorporating One .BETA.-1,4-Glucosidic Bond.

Accession number;04A0258615
Title;Synthesis and Inclusion Ability of New Cyclodextrin Analogues Incorporating One .BETA.-1,4-Glucosidic Bond.
Author; KIKUZAWA AKIRA (Osaka Univ., Grad. Sch.) KIDA TOSHIYUKI (Osaka Univ., Grad. Sch.) NAKATSUJI YOJI (Osaka Univ., Grad. Sch.) AKASHI MITSURU (Osaka Univ., Grad. Sch.)
Journal Title;Abstracts. Symposium on Biofunctional Chemistry
Journal Code:L0836A
ISSN:
VOL.18th;NO.;PAGE.64-65(2003)
Figure&Table&Reference;TBL.1, REF.3
Pub. Country;Japan
Language;Japanese
Abstract;We report here a facile synthesis of new 'skeleton-modified' CDs, in which one .ALPHA.-1,4-glucosidc bond of permethylated .ALPHA.- and .BETA.-CDs is replaced by .BETA.-1,4-glucosidic bond, and their inclusion ability toward aromatic guest compounds. Interestingly, the synthesized host molecules showed inclusion selectivity for the m-isomer over the p-isomer, in contrast to the cases of the permethylated CDs with the p-isomer selectivity. (author abst.)