Volume 30, Number 1, February 1990

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  Alan Gelberg: William Joseph Wiswesser. 1
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  Roger Attias, Jacques-Emile Dubois: Substructure systems: concepts and classifications. 2-7
• 
  Roberto Rozas, Hugo Fernandez: Automatic processing of graphics for image databases in science. 7-12
• 
  Gilles Klopman, Chandan Raychaudhury: Vertex indexes of molecular graphs in structure-activity relationships: a study of the convulsant-anticonvulsant activity of barbiturates and the carcinogenicity of unsubstituted polycyclic aromatic hydrocarbons. 12-19
• 
  Ad H. M. Thiers, Jan H. Noordik, J. Boerhout: Use of vector processing to search the Cambridge Structural Database. 19-22
• 
  Kei Takeuchi, Chiaki Kuroda, Masaru Ishida: Prolog-based functional group perception and calculation of 1-octanol/water partition coefficients using Rekker's fragment method. 22-26
• 
  Harry P. Schultz, Emily B. Schultz, Tor P. Schultz: Topological organic chemistry. 2. Graph theory, matrix determinants and eigenvalues, and topological indexes of alkanes. 27-29
• 
  Dusanka Janezic, Matej Penca, B. B. Lide, David R. Lide: Graphical handling of wide-ranging data: graphing of photon cross-section data. 30-32
• 
  Richard L. M. Synge: 25 Years of Science Citation Index - some experiences. 33-35
• 
  Richard G. Lawson, Peter C. Jurs: New index for clustering tendency and its application to chemical problems. 36-41
• 
  Nathan M. Lacoff, James E. Franke, Joseph T. Warden: Time-resolved EPR spectroscopy in a Unix environment. 42-48
• 
  Melvin L. Spann, Miriam L. Perkins: CHEMLEARN: microcomputer-based training for CHEMLINE, an alternative to formal classroom training. 48-52
• 
  Jerry Ray Dias: Isomer enumeration and topological characteristics of benzenoid quinones. 53-61
• 
  Jerry Ray Dias: Benzenoid series having a constant number of isomers. 61-64
• 
  Ramaswamy Nilakantan, Norman Bauman, Kevin S. Haraki, R. Venkataraghavan: A ring-based chemical structural query system: use of a novel ring-complexity heuristic. 65-68
• 
  Seymour B. Elk: Interpretation of Kuratowski's theorem in graph theory as both a topological abstraction and a chemical reality. 69-72
• 
  Thomas F. Kaltenbach, Gary W. Small: Determination of structural similarity by quantitative comparisons of Wiswesser Line Notation entries. 73-80
• 
  John M. Barnard: Draft specification for revised version of the Standard Molecular Data (SMD) Format. 81-96

Volume 30, Number 2, May 1990

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  Vladimir Kvasnicka, Jiri Pospichal: Canonical indexing and constructive enumeration of molecular graphs. 99-105
• 
  Cheng Qian, William Fisanick, Dale E. Hartzler, Steven W. Chapman: Enhanced algorithm for finding the smallest set of smallest rings. 105-110
• 
  Gerard Carrier, Annick Panaye, Jacques-Emile Dubois: Topological structural information in the CAS file: statistical occurrences of DARC concentric fragments. 1. Basic carbon substructures. 110-121
• 
  D. I. Cooke-Fox, G. H. Kirby, M. R. Lord, J. D. Rayner: Computer translation of IUPAC systematic organic chemical nomenclature. 4. Concise connection tables to structure diagrams. 122-127
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  D. I. Cooke-Fox, G. H. Kirby, M. R. Lord, J. D. Rayner: Computer translation of IUPAC systematic organic chemical nomenclature. 5. Steroid nomenclature. 128-132
• 
  Donald F. Averill, Kristi C. Baird, Laura L. Hopkins, Mark J. Yerkes: Fourier transform infrared spectroscopy without an FTIR spectrometer: library searching and concise storage of spectra. 133-136
• 
  Richard G. Lawson, Peter C. Jurs: Cluster analysis of acrylates to guide sampling for toxicity testing. 137-144
• 
  William Fisanick: The Chemical Abstract's Service generic chemical (Markush) structure storage and retrieval capability. 1. Basic concepts. 145-154
• 
  Paul A. D. de Maine, B. C. Cartee, M. S. Wojtyna, Margaret M. de Maine: Computer tool kit for chemists. 1. Design considerations for interfaces. 155-159
• 
  Jan V. Knop, Wolfgang R. Mueller, Klaus Szymanski, Nenad Trinajstic: Use of small computers for large computations: enumeration of polyhex hydrocarbons. 159-160
• 
  Wolfgang R. Mueller, Klaus Szymanski, Jan V. Knop, Nenad Trinajstic: Molecular topological index. 160-163
• 
  C.-S. Ai, Paul E. Blower Jr., Robert H. Ledwith: Extraction of chemical reaction information from primary journal text. 163-169
• 
  Guenter Poetzscher, A. J. C. Wilson: User needs in chemical information. 169-173
• 
  Richard B. Davidson, S. Scott Zimmerman: CONTOUR, a general contour-plotting program for IBM-compatible microcomputers, and its application to peptides. 174-177
• 
  Arleen N. Somerville: Perspectives and criteria for chemical information instruction. 177-181
• 
  Arthur A. Eggert, Catherine H. Middlecamp, Elizabeth Kean: An oxidation number assignment expert for CHEMPROF. 181-187
• 
  Gerta Rücker, Christoph Rücker: Computer perception of constitutional (topological) symmetry: TOPSYM, a fast algorithm for partitioning atoms and pairwise relations among atoms into equivalence classes. 187-191
• 
  Martin G. Hicks, Clemens Jochum: Substructure search systems. 1. Performance comparison of the MACCS, DARC, HTSS, CAS Registry MVSSS, and S4 substructure search systems. 191-199

Volume 30, Number 3, August 1990

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  Huixiao Hong, Xin Xinquan: ESSESA: an expert system for elucidation of structures from spectra. 1. Knowledge base of infrared spectra and analysis and interpretation programs. 203-210
• 
  Sven J. Cyvin, Jon Brunvoll, Bjørg N. Cyvin: Enumeration and classification of coronoid hydrocarbons. 10. Double coronoids. 210-222
• 
  Gordon M. Crippen, Timothy F. Havel: Global energy minimization by rotational energy embedding. 222-227
• 
  Carus Behnke, Joachim Bargon: Computer-assisted topological analysis and completion of chemical reactions. 228-237
• 
  David Weininger: SMILES, 3. DEPICT. Graphical depiction of chemical structures. 237-243
• 
  Sandor Barcza, Lawrence A. Kelly, Christopher D. Lenz: Computerized retrieval of information on biosynthesis and metabolic pathways. 243-251
• 
  Jerry Ray Dias: Benzenoid series having a constant number of isomers. 2. Topological characteristics of strictly pericondensed constant-isomer benzenoid series. 251-256
• 
  Zhihong Xu, Qian Dong, Xinjian Yan, Xiaoxia Li, Li Guo: The knowledge-based organic physical property data system (KB-OPDS). 256-263
• 
  Xiaoyu Liu, Krishnan Balasubramanian, Morton E. Munk: Computational techniques for vertex partitioning of graphs. 263-269
• 
  Shin-ichi Nakayama, Katsuko Sugai, Yuriko Hotate, Masayuki Yoshida: Simple and fast search system for closely related proteins. 269-271
• 
  Marianne C. Brogan, Lorrin Garson: Requirements for and challenges associated with submission of machine-readable manuscripts. 271-277
• 
  I. P. Bangov: Computer-assisted structure generation from a gross formula. 3. Alleviation of the combinatorial problem. 277-289
• 
  Jacques-Emile Dubois, G. Mathieu, P. Peguet, Annick Panaye, Jean-Pierre Doucet: Simulation of infrared spectra: an infrared spectral simulation program (SIRS) which uses DARC topological substructures. 290-302
• 
  M. Leonor Contreras, Carlos Allendes, L. Tomas Alvarez, Roberto Rozas: Computational perception and recognition of digitized molecular structures. 302-307
• 
  N. Ghoshal: Yet another linear notation scheme for organic compounds. 1. 308-311
• 
  N. W. Murrall, E. Keith Davies: Conformational freedom in 3-D databases. 1. Techniques. 312-316
• 
  Andrew R. Leach, Daniel P. Dolata, Keith Prout: Automated conformational analysis and structure generation: algorithms for molecular perception. 316-324
• 
  J. L. Wisniewski: AUTONOM: system for computer translation of structural diagrams into IUPAC-compatible names. 1. General design. 324-332
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  Michel Petitjean, Jacques-Emile Dubois: Topological statistics on a large structural file. 332-343

Volume 30, Number 4, November 1990

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  Michael F. Lynch, Peter Willett: George Vladutz, 1928-1990. 349
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  Bonnie Lawlor: George Vladutz - Obituary. 350
• 
  Martin G. Hicks: Reactions in the Beilstein information system: nonaporic organic synthesis. 352-359
• 
  Engelbert Zass: A user's view of chemical reaction information sources. 360-372
• 
  Timothy Clark: Can we predict reactivity using MO calculations? 373-376
• 
  Rainer Herges: Reaction planning: prediction of new organic reactions. 377-383
• 
  Andreas Barth: Status and future developments of reaction databases and online retrieval systems. 384-393
• 
  James E. Blake, Robert C. Dana: CASREACT: more than a million reactions. 394-399
• 
  Axel Parlow, Christian Weiske, Johann Gasteiger: ChemInform - an integrated information system on chemical reactions. 400-402
• 
  James B. Hendrickson, Todd M. Miller: Reaction indexing for reaction databases. 403-408
• 
  V. Palm: Computer-managed automatic data retrieval and prognosis system for rate and equilibrium constants of organic reactions. 409-412
• 
  Stephen Hanessian, Jonathan Franco, Gilbert Gagnon, Dominic Laramee, Benoit Larouche: Computer-assisted analysis and perception of stereochemical features in organic molecules using the CHIRON program. 413-425
• 
  Alexander J. Lawson, Hartmut Kallies: Multistep reactions: the RABBIT approach. 426-430
• 
  John E. Mills, Barbara Baughman: REACCS in the chemical development environment. 3. Graphically nonequivalent representations of molecules and reactions. 431-435
• 
  M. Takahashi, I. Dogane, M. Yoshida, H. Yamachika, T. Takabatake, Malcolm Bersohn: The performance of a noninteractive synthesis program. 436-441
• 
  Yi Zou, Mark A. Johnson, Chun Che Tsai: Modeling aromatic nitration reactions using graph-theoretic transforms. 442-450
• 
  Fulvia Orsini, Guido Sello: Geometric requirements for reactivity: the simulation of access to reaction centers and the influence of atomic deformation on it. 451-457
• 
  Ellen R. Laird, William L. Jorgensen: Computer assisted analysis of reactions involving organic free radicals and diradicals. 458-466
• 
  Johann Gasteiger, Mario Marsili, M. G. Hutchings, Heinz Saller, P. Loew, P. Roese, K. Rafeiner: Models for the representation of knowledge about chemical reactions. 467-476
• 
  David W. Elrod, Gerald M. Maggiora, Robert G. Trenary: Applications of neural networks in chemistry. 1. Prediction of electrophilic aromatic substitution reactions. 477-484
• 
  Ivar Ugi, Bernhard Gruber, Natalie Stein, Anton Demharter: Set-valued maps as a mathematical basis of computer assistance in stereochemistry. 485-489
• 
  A. Weise: Synthesis simulation by synthon substitution. 490-491
• 
  Herbert L. Gelernter, J. Royce Rose, Chyouhwa Chen: Building and refining a knowledge base for synthetic organic chemistry via the methodology of inductive and deductive machine learning. 492-504
• 
  Edward S. Blurock: Computer-aided synthesis design at RISC-Linz: automatic extraction and use of reaction classes. 505-510
• 
  Guenter Grethe, Thomas E. Moock: Similarity searching in REACCS. A new tool for the synthetic chemist. 511-520

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