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.
Publications
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.
54
Chiral asymmetrical crown-ethers, (D. A. Laidler, J. F. Stoddart), Carbohydr. Res. 1977, 55, C1-C4.
53
1,6,13,25,30 – Hexaoxa [6.6.6] (1,3,5) cyclophane. Attempted synthesis of a [4]cryptand, (W. D. Curtis, J. F. Stoddart, and G. H. Jones), J. Chem. Soc., Perkin Trans. 1 1977, 7, 785-788.
52
Macrobicyclic polyethers with bridgehead carbon atoms, (A. C. Coxon, J. F. Stoddart), J. Chem. Soc., Perkin Trans. 1 1977, 7, 767-785.
51
The trans,anti,trans- and trans,syn,trans- isomers of dicyclohexyl-18-crown-6 and their complexes, (I. J. Burden, A. C. Coxon, J. F. Stoddart, and C. M. Wheatley), J. Chem. Soc., Perkin Trans. 1 1977, 3, 220-226.
50
Conformational studies on twelve-membered heterocycles. Crystal structure of 5,18 – dimethyl – 5,18 – diazatribenzo[a,e,i] – cyclododecene – 6,17(5H,18H) – dione, (W. D. Ollis, J. S. Stephanatou, J. F. Stoddart, A. Quick, D. Rogers, and D. J. Williams), Angew. Chem. Int. Ed. Engl. 1976, 15, 757-759.
49
Chiral crowns incorporating pyridyl units and tertiary amine functions, (D. A. Laidler, J. F. Stoddart), J. Chem. Soc., Chem. Commun. 1976, 23, 979-980.
48
Enantiomeric differentiation by chiral macrocyclic polyethers derived from D-mannitol and binaphthol, (W. D. Curtis, R. M. King, J. F. Stoddart, and G. H. Jones), J. Chem. Soc., Chem. Commun. 1976, 8, 284-285.
47
Conformational behaviour of medium-sized rings. Part III. Heterocyclic analogues of 12,13 – dihydro – 11H – dibenzo[a,e]cyclononene, 6,11,12,13 – tetrahydro – 5H – dibenzo[a,e]cyclononene, and 5,6,7,12,13,14 – hexahydrodibenzo – [a,f]cyclodecene, (W. D. Ollis, J. F. Stoddart), J. Chem. Soc., Perkin Trans. 1 1976, 9, 926-937.
