Lock and key chemistry with crown compounds, (A. C. Coxon, W. D. Curtis, D. A. Laidler, J. F. Stoddart), in Asymmetry in Carbohydrates (ed. R.E. Harmon), Marcel Dekker, New York1979, 6, 167-197.
The synthesis of a chiral receptor molecule containing three carbohydrate residues within a 20-crown-6 constitution, (D. G. Andrews, P. R. Ashton, D. A. Laidler, J. F. Stoddart, and J. B. Wolstenholme), Tetrahedron Lett.1979, 20, 2629-2632.
The complexing properties of a chiral 18-crown-6 derivative incorporating a 2,5-anhydro-D-mannitol residue. A constitutional and stereochemical means of enhancing complexation, (J. A. Haslegrave, J. F. Stoddart, and D. J. Thompson), Tetrahedron Lett.1979, 20, 2279-2282.
Chiral symmetric crowns incorporating the 4,6-O-benzylidene derivatives of methyl – alpha – D – glucopyranoside and methyl – alpa-D – galactopyranoside. A configurational impediment to complexation of organic cations by 18-crown-6 derivatives, (D. A. Laidler, J. F. Stoddart, and J. B. Wolstenholme), Tetrahedron Lett.1979, 20, 465-468.
Chiral asymmetric crowns incorporating the 4,6-O-benzylidene derivatives of methy l- alpha – D – mannopyranoside and methyl – alpha – D -altropyranoside. The influence of stereochemistry upon complexation of organic cations, (R. B. Pettman, J. F. Stoddart), Tetrahedron Lett.1979, 20, 461-464.
Complexation selectivity by chiral asymmetric crowns incorporating the 4,6-O-benzylidene derivatives of methyl – alpha – D – glucopyranoside and methyl – alpha – D – galacto-pyranoside. A secondary anomeric effect, (R. B. Pettman, J. F. Stoddart), Tetrahedron Lett.1979, 20, 457-460.
The complexing properties of chiral crown ethers incorporating 1,3:4,6 – di- O – methylene – D – mannitol residues. A secondary dipole-induced dipole interaction, (D. A. Laidler, J. F. Stoddart), Tetrahedron Lett.1979, 20, 453-456.