Three aspects of an absolute configuration on the basis of the stereoisogram approach and revised terminology on related stereochemical concepts
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Cites work
- scientific article; zbMATH DE number 5015712 (Why is no real title available?)
- scientific article; zbMATH DE number 5251307 (Why is no real title available?)
- scientific article; zbMATH DE number 2239305 (Why is no real title available?)
- scientific article; zbMATH DE number 2239320 (Why is no real title available?)
- Integrated discussion on stereogenicity and chirality for restructuring stereochemistry
- Itemized enumeration of quadruplets of RS-stereoisomers under the action of RS-stereoisomer\-ic groups
- Stereoisograms for specifying chirality and RS-stereogenicity. A versatile tool for avoiding the apparent inconsistency between geometrical features and RS-nomenclature in stereochemistry
- Substitution criteria based on stereoisograms to determine prochirality and pro-RS-stereogenic\-ity
- Symmetry and combinatorial enumeration in chemistry.
- Symmetry-itemized enumeration of quadruplets of \textit{RS}-stereoisomers. I: The fixed-point matrix method of the USCI approach combined with the stereoisogram approach
- Symmetry-itemized enumeration of quadruplets of \textit{RS}-stereoisomers. II. The partial-cycle-index method of the USCI approach combined with the stereoisogram approach
Cited in
(7)- Stereoisograms for three-membered heterocycles. II: Chirality, \textit{RS}-stereogenicity, and \textit{ortho}-stereogenicity on the basis of the proligand-promolecule model
- Stereoisograms for three-membered heterocycles. III: \textit{R/S}-stereodescriptors for characterizing the \textit{RS}-stereogenic aspect of absolute configuration
- Importance of the proligand-promolecule model in stereochemistry. II: The stereoisogram approach to stereoisomeric features of prismane derivatives
- Stereoisograms of trigonal bipyramidal compounds. I: Chirality and \(RS\)-stereogenicity free from the conventional ``chirality and ``stereogenicity
- Stereoisograms of trigonal bipyramidal compounds. II: \(RS\)-stereogenicity/\(RS\)-stereoisomerism versus stereogenicity/stereoisomerism, leading to a revised interpretation of Berry's pseudorotation
- Hierarchical enumeration of octahedral complexes by using combined-permutation representations
- Stereogenicity/astereogenicity as global/local permutation-group symmetry and relevant concepts for restructuring stereochemistry
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