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Prediction of the Basicities of Pyridines in the Gas Phase and in Aqueous Solution
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Outgoing claims: the papers this work cites, builds on, or argues with.
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Application of AIM Parameters at Ring Critical Points for Estimation of π‐Electron Delocalization in Six‐Membered Aromatic and Quasi‐Aromatic Rings
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Calculation of the average properties of atoms in molecules. II
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Structure–basicity relationships for pyridine extractants
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Properties of a Ring Critical Pointas Measures of Intramolecular H-Bond Strength
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Prediction of basicity constants of various pyridines in aqueous solution using a principal component-genetic algorithm-artificial neural network
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Gaussian process: an alternative approach for QSAM modeling of peptides
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Encyclopedia of Computational Chemistry
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Substitution effects on neutral and protonated pyridine derivatives along the periodic table
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Performance of some variable selection methods when multicollinearity is present
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QSAR models based on quantum topological molecular similarity
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Description of homoaromaticity in terms of electron distributions
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Polarizability effects on the aqueous solution basicity of substituted pyridines
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Influence of Intermolecular Hydrogen Bonds on the Tautomerism of Pyridine Derivatives
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Studies on Pyridines: I. The Basicity of Pyridine Bases
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Quantum chemical topology (QCT) descriptors as substitutes for appropriate Hammett constants
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Quantum Chemical Benchmarking, Validation, and Prediction of Acidity Constants for Substituted Pyridinium Ions and Pyridinyl Radicals
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