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Publications

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.
46
The conformational behaviour of 5,6,7,12 – tetrahydrodibenzo – [a,d]cyclo – octene, (F. E. Elhadi, W. D. Ollis, and J. F. Stoddart), Angew. Chem. Int. Ed. Engl. 1976, 15, 224-225.
45
The isolation of conformational diastereoisomers of N,N’,N”- tribenzyltri – anthranilide, (W. D. Ollis, J. S. Stephanatou, J. F. Stoddart, and A. G. Ferrige), Angew. Chem. Int. Ed. Engl. 1976, 15, 223-224.
44
The use of symmetry and carbohydrates in the design of cryptands, (W. D. Curtis, D. A. Laidler, and J. F. Stoddart), Abstracts of Centennial Amer. Chem. Soc. Mtg., New York 1976, , CARB 54.
43
Stereochemistry in Sheffield, (J. F. Stoddart), Chem. Br. 1975, 13, 369.
42
Synthesis of a [2]cryptand with carbon bridgeheads, (A. C. Coxon, J. F. Stoddart), Carbohydr. Res. 1975, 44, C1-C4.
41
Chiral recognition by configurationally chiral cryptands, (W. D. Curtis, G. H. Jones, D. A. Laidler, and J. F. Stoddart), J. Chem. Soc., Chem. Commun. 1975, 20, 835-837.
40
Synthesis of configurationally chiral cryptands and cryptates from carbohydrate precursors, (W. D. Curtis, G. H. Jones, D. A. Laidler, and J. F. Stoddart), J. Chem. Soc., Chem. Commun. 1975, 20, 833-835.
39
The stereochemistry of 2,4- and 2,3 – disubstituted – gamma – butyrolactones, (S. A. M. T. Hussain, W. D. Ollis, C. Smith, and J. F. Stoddart), J. Chem. Soc., Perkin Trans. 1 1975, 15, 1480-1492.
38
Isomerism in bicyclic diacetals. Part II. Bicyclic methylene diacetals in the galacto, arabino, and ribo series, (I. J. Burden, J. F. Stoddart), J. Chem. Soc., Perkin Trans. 1 1975, 7, 675-682.
37
Isomerism in bicyclic diacetals. Part I. 1,3:2,4- and 1,4:2,3 – di – O – methylene – erythritol, (I. J. Burden, J. F. Stoddart), J. Chem. Soc., Perkin Trans. 1 1975, 7, 666-674.
36
The synthesis and conformational behaviour of N,N’,N”- trimethyltrianthranilide, (W. D. Ollis, J. A. Price, J. S. Stephanatou, and J. F. Stoddart), Angew. Chem. Int. Ed. Engl. 1975, 14, 169.
35
The conformational behaviour of 6H,12H,18H – 5,11,17 – trithiatribenzo [a,e,i] cyclo – dodecene, (W. D. Ollis, M. Nogradi, and J. F. Stoddart), Angew. Chem. Int. Ed. Engl. 1975, 14, 168-169.
34
Conformational studies on oxa, thia, and aza derivatives of 7,8,13,14 – tetrahydro – benzo [1,2] cyclonona [5,6,7-de] naphthalene and 8H,15H – 7,16 – dioxacyclodeca – [1,2,3-de : 6,7,8-d’e’] dinaphthalene, (D. J. Brickwood, W. D. Ollis, and J. F. Stoddart), Angew. Chem. Int. Ed. Engl. 1974, 13, 731-732.
33
Conformational studies on aza and thia derivatives of 6,11,12,13 – tetrahydro – 5H – dibenzo [a,f] cyclononene and 5,6,7,12,13,14 – hexahydrodibenzo[a,f]cyclodecene, (W. D. Ollis, J. F. Stoddart), Angew. Chem. Int. Ed. Engl. 1974, 13, 730-731.
32
Conformational studies on aza and thia derivatives of 12,13 – dihydro – 11H – dibenzo [a,e] cyclononene, (W. D. Ollis, J. F. Stoddart), Angew. Chem. Int. Ed. Engl. 1974, 13, 728-729.
31
Configurational equilibria in 2,4 – disubstituted – gamma – butyrolactones, (S. A. M. T. Hussain, W. D. Ollis, C. Smith, and J. F. Stoddart), J. Chem. Soc., Chem. Commun. 1974, 21, 873-874.