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.
Chiral crowns incorporating pyridyl units and tertiary amine functions, (D. A. Laidler, J. F. Stoddart), J. Chem. Soc., Chem. Commun.1976, 23, 979-980.
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.
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. 11976, 9, 926-937.
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.
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.
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 York1976, , CARB 54.
