Conformational behaviour and inclusion compound forming properties of 5,18 – disubstituted derivatives of 5,11,12,18 – tetrahydrotribenzo[b,f,j] [1,4] – diazacyclo – dodecine – 6,17 – dione, (W. D. Ollis, J. S. Stephanatou, J. F. Stoddart, G. Unal, and D. J. Williams), Tetrahedron Lett.1981, 22, 2225-2228.
Synthesis of crown ethers and analogs, (D. A. Laidler, J. F. Stoddart), in the Chemistry of the Functional Groups. Supplement E1: The Chemistry of Ethers, Crown Ethers, Hydroxyl Groups and Their Sulfur Analogs (ed. S. Patai), Wiley-Interscience1981, , 1-57.
Synthesis and conformational behaviour of 1,9,17 – triaza [2.2.2] metacyclophane – 2,10,18 – trione derivatives, (F. E. Elhadi, W. D. Ollis, J. F. Stoddart, D. J. Williams, and K. A. Woode), Tetrahedron Lett.1980, 21, 4215-4218.
Synthesis and conformational behaviour of tetra-anthranilides, (A. Hoorfar, W. D. Ollis, J. F. Stoddart, and D. J. Williams), Tetrahedron Lett.1980, 21, 4211-4214.
Dithiosalicylides and trithiosalicylides. Their conformational behaviour in solution, (G. B. Guise, W. D. Ollis, J. A. Peacock, J. S. Stephanatou, and J. F. Stoddart), Tetrahedron Lett.1980, 21, 4203-4206.
Old crowns and new chemistry: Molecular receptors and intermolecular conformational analysis, (J. F. Stoddart), Lectures in Heterocyclic Chemistry, Vol. 5 (ed. R.N. Castle and S.W. Schneller)1980, , S-47-S-60.
High resolution 13C NMR spectroscopy and X-ray crystallography of complexes formed by N,N’ – dimethyl – 1,7 – diaza – 4,10 – dioxacyclododecane, (J. C. Metcalfe, J. F. Stoddart, G. Jones, W. E. Hull, A. Atkinson, I. S. Kerr, and D. J. Williams), J. Chem. Soc., Chem. Commun.1980, 12, 540-543.
Holes, handedness, handles, and hopes – meeting the requirements of primary binding, chirality, secondary binding, and functionality in enzyme analogues, (J. F. Stoddart), in Proceedings of the Summer School on Bioenergetics and Thermodynamics: Model systems, 21 May - 1 June 1979, Tabiano, Italy (ed. A. Braibanti), Reidel, Dorcrecht, Holland1980, , 43-62.
The design and development of enzyme analogues, (J. F. Stoddart), in Enzymic and Non-Enzymic Catalysis (ed. P. Dunnill, A. Wiseman, and N. Blakebrough), Ellis Horwood, Chichester1980, , 84-110.
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.
