posted on 2015-01-02, 00:00authored byJunya Nishiyama, Yoshimasa Makita, Nobuhiro Kihara
Secondary ammonium salts bearing
a cyclopentyl terminal group rapidly formed pseudorotaxane with 1.5
equiv of DB24C8. Acylation of the pseudorotaxane with 50 equiv of
benzoyl chloride in the presence of 50 equiv of triethylamine in toluene
afforded rotaxane, the product of active transport, in 95% yield.
The cyclopentyl group is small enough to allow rapid formation of
pseudorotaxane, and bulky enough to facilitate the quantitative active
transport by steric repulsion.