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Publications

84
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-Interscience 1981, , 1-57.
83
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.
82
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.
81
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.
80
Enzymes to order?, (J. F. Stoddart), in Spectrum (ed. M.J. Quan) published by The Central Office of Information, London 1980, 170, 5-7.
79
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.
78
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.
77
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, Holland 1980, , 43-62.
76
The synthesis and complexing properties of oxo-12-crown-3 and oxo-18-crown-5, (G. D. Beresford, J. F. Stoddart), Tetrahedron Lett. 1980, 21, 867-870.
75
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, Chichester 1980, , 84-110.
74
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 York 1979, 6, 167-197.
73
From carbohydrates to enzyme analogues (Tate and Lyle Lecture), (J. F. Stoddart), Chem. Soc. Rev. 1979, 8, 85-142.
72
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.
71
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.
70
Nomenclature and stereochemistry, (J. F. Stoddart), in Barton and Ollis's Comprehensive Organic Chemistry, Vol. 1 (ed., J.F. Stoddart), Pergamon Press, Oxford 1979, 1, 3-33.
69
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.
68
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.
67
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.
66
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.
65
Stereochemistry of noncovalent interactions in organic and metal cationic complexes, (A. C. Coxon, D. A. Laidler, R. B. Pettman, and J. F. Stoddart), J. Am. Chem. Soc. 1978, 100, 8260-8262.
64
Conformational behaviour of medium-sized rings. Part 8. 6H,12H,18H – Tribenzo [b,f,j] [1,5,9] trithiacyclododecin and its 5,5,11,11,17,17 – hexaoxide, (W. D. Ollis, J. S. Stephanatou, J. F. Stoddart, and M. Nogradi), J. Chem. Soc., Perkin Trans. 1 1978, 11, 1421-1428.
63
Conformational behaviour of medium-sized rings. Part 7. 5,6,7,12 – Tetrahydro – dibenzo[a,d]cyclo – octene, (F. E. Elhadi, W. D. Ollis, and J. F. Stoddart), J. Chem. Soc., Perkin Trans. 1 1978, 11, 1415-1421.
62
Conformational behaviour of medium-sized rings. Part 6. 5,6,11,12,17,18 – Hexahydrotribenzo [a,e,i]cyclododecene and its 2,3,8,9,14,15 – and 1,4,7,10,13,16 – hexamethyl derivatives. 2,3,8,9 – and 1,4,7,10 – Tetramethyl – 5,6,11,12 – tetrahydrodibenzo[a,e], (D. J. Brickwood, W. D. Ollis, J. S. Stephanatou, and J. F. Stoddart), J. Chem. Soc., Perkin Trans. 1 1978, 11, 1389-1414.
61
Conformational behaviour of medium-sized rings. Part 5. Transannular reactions of (16Z) – 8,9 – dihydro – 8 – methyl – 17H – dinaphth [1,8-cd:1′,8′-hi] azacycloundecine and (12Z) – 6,7 – dihydro – 6 – methyl – 5H – benz[cg]azonine. Two examples of “revers, (D. J. Brickwood, A. M. Hassan, W. D. Ollis, J. S. Stephanatou, and J. F. Stoddart), J. Chem. Soc., Perkin Trans. 1 1978, 11, 1393-1398.
60
Conformational behaviour of medium-sized rings. Part 4. Heterocyclic analogues of 7,8,13,14-tetrahydrobenzo[6,7]cyclonona[1,2,3-de]naphthalene and 7,8,15,16 – tetrahydrocyclodeca [1,2,3-de:6,7,8-d’e’] dinaphthalene, (D. J. Brickwood, W. D. Ollis, and J. F. Stoddart), J. Chem. Soc., Perkin Trans. 1 1978, 11, 1385-1392.
59
Complexes of primary alkylammonium salts and secondary dialkylammonium salts with diazaparacyclophanes, (H. F. Beckford, R. M. King, J. F. Stoddart, and R. F. Newton), Tetrahedron Lett. 1978, 19, 171-174.
58
The complexation of primary alkylammonium salts and secondary dialkyl – ammonium salts by N,N – dimethyl – 1,7 – diaza – 4,10 – dioxacyclodecane, (J. C. Metcalfe, J. F. Stoddart, and G. H. Jones), J. Am. Chem. Soc. 1977, 99, 8317-8319.
57
To enzyme analogues by lock and key chemistry with crown compounds. Part 1. Enantiomeric differentiation by configurationally chiral cryptands synthesised from L-tartaric acid and D-mannitol, (W. D. Curtis, D. A. Laidler, J. F. Stoddart, and G. H. Jones), J. Chem. Soc., Perkin Trans. 1 1977, 15, 1756-1770.
56
Enantiomeric differentiation by a chiral symmetrical crown derived from L-iditol, (W. D. Curtis, D. A. Laidler, J. F. Stoddart, J. B. Wolstenholme, and G. H. Jones), Carbohydr. Res. 1977, 57, C17-C22.
55
Stereoselectivity in complexation of primary alkylammonium cations by the diastereotopic faces of chiral asymmetric crowns, (D. A. Laidler, J. F. Stoddart), J. Chem. Soc., Chem. Commun. 1977, 14, 481-483.