H. Ikeda et al., Artificial holoenzymes for benzoin condensation using thiazolio-appended beta-cyclodextrin dimers, TETRAHEDR L, 41(33), 2000, pp. 6483-6487
Artificial holoenzymes for benzoin condensation were synthesized using thia
zolio-appended beta-cyclodextrin dimers. The dimer with an L-aspartic acid
residue as a linker for connecting two beta-cyclodextrin units caused a 26-
fold acceleration in the benzoin condensation, whereas the dimer with the l
inker of a L-glutamic acid residue caused only a 7-fold acceleration, indic
ating that the linker length of the dimer is an important factor in this ar
tificial holoenzyme. (C) 2000 Elsevier Science Ltd, All rights reserved.