Size discrimination in intramolecular complexation of modified α-cyclodextrins: a preparative and nuclear magnetic resonance study

摘要

Acylation of the primary amine group of 6A-(6-aminohexylamino)-6A-deoxy-α-cyclodextrin 1 by 4-nitrophenylntrinorbornane-2-acetate 6, 1-methoxycarbonyl-8-(4-nitrophenoxycarbonyl)cubane 7, 1-methoxycarbonyl-2,3-ndimethyl-8-(4-nitrophenoxycarbonyl)cubane 8, and 1-(4-nitrophenoxycarbonyl)adamantane 9, respectively, givesn6A-deoxy-[6-(trinorbornan-2-ylacetylamino)hexylamino]-α-cyclodextrin 2, 6A-[6-(8-carboxycuban-1-ylcarbonylamino)nhexylamino]-6A-deoxy-α-cyclodextrin 3, 6A-[6-(8-carboxy-2,3-dimethylcuban-l-ylcarbonylamino)hexylamino]-n6A-deoxy-α-cyclodextrin 4, and 6A-[6-(adamantan-1-ylcarbonylamino)hexylamino]-6A-deoxy-α-cyclodextrin 5, inngood yields together with 4-nitrophenolate. In basic D2O, the substituents of 1–4 complex intramolecularly withinnthe α-cyclodextrin annulus, whereas that of 5 does not due to its larger size, as shown by 1H ROESY NMRnspectroscopy. This facilitates a mechanistic comparison with the formation of βCD analogues of 2–5.