Journal of Organic Chemistry p. 1837 - 1839 (1988)
Update date:2022-08-03
Topics:
Tee, Oswald S.
Du, Xian-xian
The kinetics of ester cleavage of 4-carboxy-2-nitrophenyl alkanoates (C2, C4, C6, C7, C8) in aqueous base containing α- or β-cyclodextrin (α- or β-CD) indicate that for the three longer esters there are processes involving two CD molecules which are quite distinct: with α-CD a 2:1 binding leads to inhibition; with β-CD a second-order process provides catalysis.
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