Cyclopropylcarboxamidinium chloride.

J.Barker, H.R.Powell, Acta Crystallogr. ,Sect. C:Cryst. Struct. Commun., 1998, 54 1189-1191, DOI: 10.1107/S0108270197018829

Mechanistic and synthetic aspects of stereoselective reactions of lithium derivatives of chiral phosphine oxides: X-ray crystal structure of (1R*,2S*,1 ' S*.2 'R*)-1-(1'-diphenylphosphinoyl-2'-phenylpropyl)-2- phenylsulfanylcyclohexan-1-ol.

C.Gueguen, P.O'Brien, H.R.Powell, P.R.Raithby, S.Warren, J. Chem. Soc. ,Perkin Trans. 1, 1998, 3405-3417, DOI: 10.1039/a805354e

S-benzylisothiouronium chloride.

J.Barker, H.R.Powell, Acta Crystallogr. ,Sect. C:Cryst. Struct. Commun., 1998, 54 2019-2021, DOI: 10.1107/S0108270198008166

13C CPMAS NMR spectroscopy as a probe for porphyrin-porphyrin and host-guest interactions in the solid state.

N.Bampos, M.R.Prinsep, Heyong He, A.Vidal-Ferran, A.Bashall, M.McPartlin, H.Powell, J.K.M.Sanders, J. Chem. Soc. ,Perkin Trans. 2, 1998, 715-723, DOI: 10.1039/a704492e

A thymine-like base analogue forms wobble pairs with adenine in a Z-DNA duplex.

G. S. Schuerman, L. Van Meervelt, D. Loakes, D. M. Brown, P. Kong Thoo, P. Lon, M. H.Moore, S. A. Salisbury, J. Mol. Biol., 1998, 282 1005-1011, DOI: 10.1006/jmbi.1998.2080

Cyclisation and rearrangement of N4-acylaminodeoxycytidines.

D.Loakes, D.M.Brown, S.A.Salisbury, Tetrahedron Lett., 1998, 39 3865-3868, DOI: 10.1016/S0040-4039(98)00634-0

Use of the Cambridge Structural Database to study non-covalent interactions: Towards a knowledge-base of intermolecular interactions.

J. C. Cole, J. P. M. Lommerse, R. S. Rowland, R. Taylor, F. H. Allen, Struct. -Based Drug Discov. :An Overview, 1998, 352 113-124, DOI: 10.1007/978-94-015-9028-0_11

The Cambridge Structural Database System: Conformational analysis from crystallographic data.

F. H. Allen, N. A. Pitchford, Structure-Based Drug Design: Experimental and Computational Approaches, 1998, 352 15-26, DOI: 10.1007/978-94-015-9028-0_2

Relationships between experiment and theory in the study of intermolecular interactions.

F. H. Allen, Intermolecular Interactions, 1998, 111-120, DOI: 10.1007/978-1-4615-4829-4_10

The Cambridge Structural Database System.

F. H. Allen, V. J. Hoy, Encyclopaedia of Computational Chemistry, 1998, 1 155-167

Directional preferences of intermolecular contacts to hydrophobic groups.

J. C. Cole, R. Taylor, M. L. Verdonk, Acta Crystallogr. ,Sect. D:Biol. Crystallogr., 1998, D54 1183-1193, DOI: 10.1107/S0907444998008932

The development, status and scientific impact of crystallographic databases.

F. H. Allen, Acta Crystallogr. ,Sect. A:Found Crystallogr., 1998, A54 758-771, DOI: 10.1107/S0108767398010563

Systematic analysis of metal coordination sphere geometry from crystallographic data: a general method for detecting geometrical preferences, deformations and interconversion pathways.

J. A. K. Howard, R. C. B. Copley, J. W. Yao, F. H. Allen, Chem. Commun., 1998, 2175-2176, DOI: 10.1039/a806820h

Crystallographic databases and their use for studying intermolecular interactions.

N. A. Pitchford, R. Taylor, Designing Bioactive Molecules, 1998,

Probabilities of formation of bimolecular cyclic hydrogen-bonded motifs in organic crystal structures: a systematic database study.

F. H. Allen, P. R. Raithby, G. P. Shields, R. Taylor, Chem. Commun., 1998, 1043-1044, DOI: 10.1039/a801424h

Hydrogen-bonded interactions of thiocyanate ions: statistical and quantum-chemical analyses.

J. P. M. Lommerse, J. C. Cole, Acta Crystallogr. ,Sect. B:Struct. Sci., 1998, B54 316-319, DOI: 10.1107/S0108768197014602

Carbonyl-carbonyl interactions can be competitive with hydrogen bonds.

F. H. Allen, C. A. Balham, J. P. M. Lommerse, P. R. Raithby, Acta Crystallogr. ,Sect. B:Struct. Sci., 1998, B54 320-329, DOI: 10.1107/S0108768198001463