akis(6-O-tert-butyldimethylsilyl)beta-cyclodextrin reacts with N-methy
l-4-chloromethyl-2-nitroaniline to produce the 3-modified cyclodextrin
after the necessary deprotection step. Complete NMR assignment and it
s comparison with cyclodextrin derivatives modified by the same group
at the 2- and 6-position is reported. Copyright (C) 1996 Elsevier Scie
nce Ltd