Shinsaku Fujita
According to our database1,
Shinsaku Fujita
authored at least 29 papers
between 1986 and 2004.
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Bibliography
2004
Group-Theoretical Discussion on the <i>E</i>/<i>Z</i>-Nomenclature for Ethylene Derivatives. Discrimination between <i>RS</i>-Stereoisomeric Groups and Stereoisomeric Groups.
J. Chem. Inf. Model., 2004
2000
Characteristic Monomials with Chirality Fittingness for Combinatorial Enumeration of Isomers with Chiral and Achiral Ligands.
J. Chem. Inf. Comput. Sci., 2000
Combinatorial Enumeration of Nonrigid Isomers with Given Ligand Symmetries on the Basis of Promolecules with A Subsymmetry of Dh.
J. Chem. Inf. Comput. Sci., 2000
J. Chem. Inf. Comput. Sci., 2000
1999
J. Chem. Inf. Comput. Sci., 1999
XyM Markup Language (XyMML) for Electronic Communication of Chemical Documents Containing Structural Formulas and Reaction Schemes.
J. Chem. Inf. Comput. Sci., 1999
Benzene Derivatives with Achiral and Chiral Substituents and Relevant Derivatives Derived from D6h Skeletons. Symmetry-Itemized Enumeration and Symmetry Characterization by the Unit-Subduced Cycle Index Approach.
J. Chem. Inf. Comput. Sci., 1999
1998
Pseudo-Point Groups and Subsymmetry-Itemized Enumeration for Characterizing the Symmetries of 1, 4-Dioxane and 1, 4-Oxathiane Derivatives.
J. Chem. Inf. Comput. Sci., 1998
1997
1996
The Sphericity Concept for an Orbit of Bonds. Formulation of Chirogenic Sites in a Homospheric Orbit and of Bond-Differentiating Chiral Reactions with Applications to C60-Adducts.
J. Chem. Inf. Comput. Sci., 1996
1994
Comput. Chem., 1994
1992
Promolecules with a subsymmetry of D.infin.h. Combinatorial enumeration and stereochemical properties.
J. Chem. Inf. Comput. Sci., 1992
1991
J. Chem. Inf. Comput. Sci., 1991
1989
Formulation of isomeric reaction types and systematic enumeration of six-electron pericyclic reactions.
J. Chem. Inf. Comput. Sci., 1989
1988
Canonical numbering and coding of reaction center graphs and reduced reaction center graphs abstracted from imaginary transition structures. A novel approach to the linear coding of reaction types.
J. Chem. Inf. Comput. Sci., 1988
Canonical numbering and coding of imaginary transition structures. A novel approach to the linear coding of individual organic reactions.
J. Chem. Inf. Comput. Sci., 1988
A new algorithm for selection of synthetically important rings. The essential set of essential rings for organic structures.
J. Chem. Inf. Comput. Sci., 1988
Logical perception of ring-opening, ring-closure, and rearrangement reactions based on imaginary transition structures. Selection of the essential set of essential rings (ESER).
J. Chem. Inf. Comput. Sci., 1988
1987
Structure-reaction type paradigm in the conventional methods of describing organic reactions and the concept of imaginary transition structures overcoming this paradigm.
J. Chem. Inf. Comput. Sci., 1987
Description of organic reactions based on imaginary transition structures. 9. Single-access perception of rearrangement reactions.
J. Chem. Inf. Comput. Sci., 1987
Description of organic reactions based on imaginary transition structures. 8. Synthesis space attached by a charge space and three-dimensional imaginary transition structures with charges.
J. Chem. Inf. Comput. Sci., 1987
Description of organic reactions based on imaginary transition structures. 7. Classification and enumeration of two-string reactions with two or more common nodes.
J. Chem. Inf. Comput. Sci., 1987
Description of organic reactions based on imaginary transition structures. 6. Classification and enumeration of two-string reactions with one common node.
J. Chem. Inf. Comput. Sci., 1987
1986
Description of organic reactions based on imaginary transition structures. 5. Recombination of reaction strings in a synthesis space and its application to the description of synthetic pathways.
J. Chem. Inf. Comput. Sci., 1986
Description of organic reactions based on imaginary transition structures. 4. Three-nodal and four-nodal subgraphs for a systematic characterization of reactions.
J. Chem. Inf. Comput. Sci., 1986
Description of organic reactions based on imaginary transition structures. 3. Classification of one-string reactions having an odd-membered cyclic reaction graph.
J. Chem. Inf. Comput. Sci., 1986
Description of organic reactions based on imaginary transition structures. 2. Classification of one-string reactions having an even-membered cyclic reaction graph.
J. Chem. Inf. Comput. Sci., 1986
Description of organic reactions based on imaginary transition structures. 1. Introduction of new concepts.
J. Chem. Inf. Comput. Sci., 1986