Journal of the Chemical Society. Chemical communications p. 1269 - 1274 (1993)
Update date:2022-09-26
Topics:
Ashton, Peter R.
Belohradsky, Martin
Philp, Douglas
Stoddart, J. Fraser
The exploitation of size-complementarity between the macrocyclic component and the stoppers of the cumbbell component of a <2>rotaxane, together with stabilising noncovalent bonding interactions that create a thermodynamic trap, have permitted the development of an alternative method, which can be termed slippage, for the syntheses of <2>rotaxanes in good yields.
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