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Publications

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.
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.