On the public citation graph

Topological Organic Chemistry. 9. Graph Theory and Molecular Topological Indices of Stereoisomeric Organic Compounds

0 signed · 70 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What points at this work

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

inferred← citeshttps://doi.org/10.1002/9780470027318.a1918openalex-snapshot
Quantitative Structure–Activity Relationships and Computational Methods in Drug Discovery
inferred← citeshttps://doi.org/10.1002/9780470027318.a1918.pub2openalex-snapshot
Quantitative Structure–Activity Relationships and Computational Methods in Drug Discovery
inferred← citeshttps://doi.org/10.1002/9780470027318.a1918.pub3openalex-snapshot
Quantitative Structure‐Activity Relationships and Computational Methods in Drug Discovery
inferred← citeshttps://doi.org/10.1002/9783527613106.biblioopenalex-snapshot
Bibliography
inferred← citeshttps://doi.org/10.1002/9783527618279.ch39aopenalex-snapshot
Representation of Molecular Chirality
inferred← citeshttps://doi.org/10.1002/9783527816880.ch3openalex-snapshot
Computer Processing of Chemical Structure Information
inferred← citeshttps://doi.org/10.1002/cem.2464openalex-snapshot
Methods of studies on quantitative structure–activity relationships for chiral compounds
inferred← citeshttps://doi.org/10.1002/chin.199604283openalex-snapshot
ChemInform Abstract: Topological Organic Chemistry. Part 9. Graph Theory and Molecular Topological Indices of Stereoisomeric Organic Compounds.
inferred← citeshttps://doi.org/10.1002/chin.200444298openalex-snapshot
Whole Molecule and Atom‐Based Topological Descriptors
inferred← citeshttps://doi.org/10.1002/jcc.20964openalex-snapshot
Bond‐based 3D‐chiral linear indices: Theory and QSAR applications to central chirality codification
inferred← citeshttps://doi.org/10.1002/jssc.200800693openalex-snapshot
Exploring enantioselective molecular recognition mechanisms with chemoinformatic techniques
inferred← citeshttps://doi.org/10.1002/minf.201800039openalex-snapshot
GOWAWA Aggregation Operator‐based Global Molecular Characterizations: Weighting Atom/bond Contributions (LOVIs/LOEIs) According to their Influence in the Molecular Encoding
inferred← citeshttps://doi.org/10.1002/minf.202060030openalex-snapshot
Multiple Conformer Descriptors for QSAR Modeling
inferred← citeshttps://doi.org/10.1002/ps.1116openalex-snapshot
Chirality index, molecular overlay and biological activity of diastereoisomeric mosquito repellents
inferred← citeshttps://doi.org/10.1002/qsar.200730048openalex-snapshot
Description and Application of Similarity‐Based Methods for Fast and Simple QSAR Model Development
inferred← citeshttps://doi.org/10.1002/qsar.200960085openalex-snapshot
Applications of Bond‐Based 3D‐Chiral Quadratic Indices in QSAR Studies Related to Central Chirality Codification
inferred← citeshttps://doi.org/10.1007/0-306-46907-3_1openalex-snapshot
From Chemical Graphs to 3D Molecular Modeling
inferred← citeshttps://doi.org/10.1007/7081_025openalex-snapshot
Predicting Pharmacological and Toxicological Activity of Heterocyclic Compounds Using QSAR and Molecular Modeling
inferred← citeshttps://doi.org/10.1007/978-0-387-30440-3_136openalex-snapshot
Drug Design, Molecular Descriptors in
inferred← citeshttps://doi.org/10.1007/978-0-387-30440-3_422openalex-snapshot
QSAR Modeling and QSAR Based Virtual Screening, Complexity and Challenges of Modern
inferred← citeshttps://doi.org/10.1007/978-1-4757-3273-3_2openalex-snapshot
Some Relationships between Molecular Energy-Topology and Symmetry
inferred← citeshttps://doi.org/10.1007/978-3-031-67841-7_3openalex-snapshot
Chirality Descriptors for Numerical Characterization of Enantiomers and Diastereomers
inferred← citeshttps://doi.org/10.1007/978-3-319-56850-8_2openalex-snapshot
The Use of Topological Indices in QSAR and QSPR Modeling
inferred← citeshttps://doi.org/10.1007/978-3-540-69387-1_64openalex-snapshot
Spectral Properties of Adjacency and Distance Matrices for Various Networks
inferred← citeshttps://doi.org/10.1007/978-3-642-27737-5_136-2openalex-snapshot
Drug Design, Molecular Descriptors in
inferred← citeshttps://doi.org/10.1007/s10822-005-7575-8openalex-snapshot
3D-chiral Atom, Atom-type, and Total Non-stochastic and Stochastic Molecular Linear Indices and their Applications to Central Chirality Codification
inferred← citeshttps://doi.org/10.1007/s10910-008-9386-3openalex-snapshot
3D-chiral (2.5) atom-based TOMOCOMD-CARDD descriptors: theory and QSAR applications to central chirality codification
inferred← citeshttps://doi.org/10.1007/s10910-015-0533-3openalex-snapshot
Novel global and local 3D atom-based linear descriptors of the Minkowski distance matrix: theory, diversity–variability analysis and QSPR applications
inferred← citeshttps://doi.org/10.1007/springerreference_60308openalex-snapshot
Drug Design, Molecular Descriptors in
inferred← citeshttps://doi.org/10.1016/j.asej.2025.103647openalex-snapshot
Degree-based fuzzy indices analysis of two snake graphs
inferred← citeshttps://doi.org/10.1016/j.bmc.2004.07.051openalex-snapshot
3D-Chiral quadratic indices of the ‘molecular pseudograph’s atom adjacency matrix’ and their application to central chirality codification: classification of ACE inhibitors and prediction of σ-receptor antagonist activities
inferred← citeshttps://doi.org/10.1016/j.carres.2008.03.012openalex-snapshot
Artificial neural network aided estimation of the electrochemical signals of monosaccharides on gold electrode
inferred← citeshttps://doi.org/10.1016/j.chemolab.2015.03.016openalex-snapshot
Machine learning induction of chemically intuitive rules for the prediction of enantioselectivity in the asymmetric syntheses of alcohols
inferred← citeshttps://doi.org/10.1016/j.jmgm.2006.09.007openalex-snapshot
Atom-based stochastic and non-stochastic 3D-chiral bilinear indices and their applications to central chirality codification
inferred← citeshttps://doi.org/10.1016/j.jmgm.2010.08.007openalex-snapshot
Complementing ultrafast shape recognition with an optical isomerism descriptor
inferred← citeshttps://doi.org/10.1016/j.trac.2018.05.019openalex-snapshot
Molecular modeling and prediction accuracy in Quantitative Structure-Retention Relationship calculations for chromatography
inferred← citeshttps://doi.org/10.1016/s0097-8485(02)00053-0openalex-snapshot
Symmetry considerations in Markovian chemicals ‘in silico’ design (MARCH-INSIDE) I: central chirality codification, classification of ACE inhibitors and prediction of σ-receptor antagonist activities
inferred← citeshttps://doi.org/10.1016/s0097-8485(02)00056-6openalex-snapshot
Preliminary approach to estimation and prediction of infrared spectroscopy for Mannich bases by atomic electronegativity distance vector (VAED)
inferred← citeshttps://doi.org/10.1016/s1093-3263(01)00136-xopenalex-snapshot
Prediction of enantiomeric selectivity in chromatography
inferred← citeshttps://doi.org/10.1016/s1093-3263(98)00013-8openalex-snapshot
Prediction of properties of chiral compounds by molecular topology
inferred← citeshttps://doi.org/10.1021/ci000082aopenalex-snapshot
Novel Chirality Descriptors Derived from Molecular Topology
inferred← citeshttps://doi.org/10.1021/ci000115mopenalex-snapshot
Graph Theoretical Descriptors of Two-Dimensional Chirality with Possible Extension to Three-Dimensional Chirality
inferred← citeshttps://doi.org/10.1021/ci000125nopenalex-snapshot
New Description of Molecular Chirality and Its Application to the Prediction of the Preferred Enantiomer in Stereoselective Reactions
inferred← citeshttps://doi.org/10.1021/ci000156iopenalex-snapshot
3D Connectivity Indices in QSPR/QSAR Studies
inferred← citeshttps://doi.org/10.1021/ci0003247openalex-snapshot
Molecular Electronegative Distance Vector (MEDV) Related to 15 Properties of Alkanes
inferred← citeshttps://doi.org/10.1021/ci0100402openalex-snapshot
Combination of 2D-, 3D-Connectivity and Quantum Chemical Descriptors in QSPR. Complexation of α- and β-Cyclodextrin with Benzene Derivatives
inferred← citeshttps://doi.org/10.1021/ci0103469openalex-snapshot
Novel ZE-Isomerism Descriptors Derived from Molecular Topology and Their Application to QSAR Analysis
inferred← citeshttps://doi.org/10.1021/ci020285uopenalex-snapshot
Data Mining for Seeking an Accurate Quantitative Relationship between Molecular Structure and GC Retention Indices of Alkenes by Projection Pursuit
inferred← citeshttps://doi.org/10.1021/ci034119dopenalex-snapshot
QSAR Study of Catalytic Asymmetric Reactions with Topological Indices
inferred← citeshttps://doi.org/10.1021/ci0600511openalex-snapshot
A Steroids QSAR Approach Based on Approximate Similarity Measurements
inferred← citeshttps://doi.org/10.1021/ci600235wopenalex-snapshot
Physicochemical Stereodescriptors of Atomic Chiral Centers
inferred← citeshttps://doi.org/10.1021/ci600542bopenalex-snapshot
Novel Approach for the Numerical Characterization of Molecular Chirality
inferred← citeshttps://doi.org/10.1021/ci960027vopenalex-snapshot
Topological Organic Chemistry. 10. Graph Theory and Topological Indices of Conformational Isomers
inferred← citeshttps://doi.org/10.1021/ci960168xopenalex-snapshot
From Chemical Topology to 3D Geometry
inferred← citeshttps://doi.org/10.1021/ci970019uopenalex-snapshot
Matrix Operator, W(M1,M2,M3), and Schultz-Type Indices
inferred← citeshttps://doi.org/10.1080/10629369808033259openalex-snapshot
Topological and Stereochemical Molecular Descriptors for Databases Useful in QSAR, Similarity/Dissimilarity and Drug Design
inferred← citeshttps://doi.org/10.1080/1062936x.2017.1344729openalex-snapshot
Tensor algebra-based geometric methodology to codify central chirality on organic molecules
inferred← citeshttps://doi.org/10.11606/t.85.2014.tde-12022015-142658openalex-snapshot
Estudo dos compostos bioativos em especiarias (Syzygium aromaticum L, Cinnamomum zeylanicum Blume e Myristica fragans Houtt) processadas por radiação ionizante
inferred← citeshttps://doi.org/10.1201/9780203642627.ch5openalex-snapshot
Whole Molecule and Atom-Based Topological Descriptors
inferred← citeshttps://doi.org/10.1201/9781420065442.ch31openalex-snapshot
Predicting Chemical Reactivity and Bioactivity of Molecules from Structure
inferred← citeshttps://doi.org/10.1556/jpc.16.2003.4.3openalex-snapshot
O-methyloximes of testosterone and of 17α-methyltestosterone: TLC and QSPR study ofRFvalues
inferred← citeshttps://doi.org/10.2174/1568026623666230731103309openalex-snapshot
Physicochemical Significance of Topological Indices: Importance in Drug Discovery Research
inferred← citeshttps://doi.org/10.2174/157340909787580836openalex-snapshot
Numerical Characterization of Molecular Chirality of Organic Compounds
inferred← citeshttps://doi.org/10.3109/14756366.2010.549089openalex-snapshot
Topological, hydrophobicity, and other descriptors on α-glucosidase inhibition: a QSAR study on xanthone derivatives
inferred← citeshttps://doi.org/10.3390/pr10030577openalex-snapshot
Machine Learning Prediction of Critical Temperature of Organic Refrigerants by Molecular Topology
inferred← citeshttps://doi.org/10.35537/10915/71941openalex-snapshot
Estudio, desarrollo y aplicación de modelos de la teoría QSPR-QSAR en pesticidas
inferred← citeshttps://doi.org/10.3797/scipharm.0804-12openalex-snapshot
Chemical Structure Indices in In Silico Molecular Design
inferred← citeshttps://doi.org/10.4067/s0717-97072012000100001openalex-snapshot
AN IMPROVED TOPOLOGICAL DESCRIPTOR EDm AND ITS APPLICATION
inferred← citeshttps://doi.org/10.47745/ausi-2024-0006openalex-snapshot
Vertex eccentric connectivity index of chemical graphs obtained from (a)bis(pyridine)-cobalt(III)chloride
inferred← citeshttps://doi.org/10.48550/arxiv.1303.1724openalex-snapshot
Automated Identification and Classification of Stereochemistry: Chirality and Double Bond Stereoisomerism
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.