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An Effective Topological Symmetry Perception and Unique Numbering Algorithm

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1021/c160017a019openalex-snapshot
A Connectivity Code for Use in Describing Chemical Structures.
inferredcites →https://doi.org/10.1021/ci00006a006openalex-snapshot
Automorphism and equivalence classes
inferredcites →https://doi.org/10.1021/ci00006a007openalex-snapshot
Limits of classification. 2. Comment on Lawson and Jurs
inferredcites →https://doi.org/10.1021/ci00015a009openalex-snapshot
Morgan revisited
inferredcites →https://doi.org/10.1021/ci60002a007openalex-snapshot
On Unique Numbering of Atoms and Unique Codes for Molecular Graphs
inferredcites →https://doi.org/10.1021/ci60020a015openalex-snapshot
An Approach to the Assignment of Canonical Connection Tables and Topological Symmetry Perception
inferredcites →https://doi.org/10.1021/ci60022a014openalex-snapshot
Algorithms for Unique and Unambiguous Coding and Symmetry Perception of Molecular Structure Diagram. III. Method of Subregion Analysis for Unique Coding and Symmetry Perception

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1002/0470845015.cca001openalex-snapshot
Canonical Numbering and Constitutional Symmetry
inferred← citeshttps://doi.org/10.1002/9783527613106.biblioopenalex-snapshot
Bibliography
inferred← citeshttps://doi.org/10.1002/9783527618279.ch7aopenalex-snapshot
Canonical Numbering and Constitutional Symmetry
inferred← citeshttps://doi.org/10.1002/9783527628766.biblioopenalex-snapshot
Bibliography
inferred← citeshttps://doi.org/10.1002/jcc.21843openalex-snapshot
Indexing molecules with chemical graph identifiers
inferred← citeshttps://doi.org/10.1016/s0097-8485(01)00089-4openalex-snapshot
The study on automorphism group of ESESOC
inferred← citeshttps://doi.org/10.1021/acs.jpclett.4c01751openalex-snapshot
Unsupervised Machine Learning in the Analysis of Nonadiabatic Molecular Dynamics Simulation
inferred← citeshttps://doi.org/10.1021/ci0003911openalex-snapshot
Algorithm for Naming Molecular Equivalence Classes Represented by Labeled Pseudographs
inferred← citeshttps://doi.org/10.1021/ci020343bopenalex-snapshot
Encoding of Polycyclic Si-Containing Molecules for Determining Species Uniqueness in Automated Mechanism Generation
inferred← citeshttps://doi.org/10.1021/ci600238jopenalex-snapshot
Algorithm for Advanced Canonical Coding of Planar Chemical Structures That Considers Stereochemical and Symmetric Information
inferred← citeshttps://doi.org/10.1039/d4dd00208copenalex-snapshot
MolBar: a molecular identifier for inorganic and organic molecules with full support of stereoisomerism
inferred← citeshttps://doi.org/10.1063/1.4828704openalex-snapshot
Metrics for measuring distances in configuration spaces
inferred← citeshttps://doi.org/10.1186/s13321-020-00453-4openalex-snapshot
Atomic ring invariant and Modified CANON extended connectivity algorithm for symmetry perception in molecular graphs and rigorous canonicalization of SMILES
inferred← citeshttps://doi.org/10.70675/95e970f3z6758z4c72zbc41z733e9a10dbd2openalex-snapshot
Analyse structurale automatique des petites molécules organiques
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