Stereoisograms for three-membered heterocycles. II: Chirality, \textit{RS}-stereogenicity, and \textit{ortho}-stereogenicity on the basis of the proligand-promolecule model
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Publication:2263703
DOI10.1007/S10910-014-0427-9zbMATH Open1307.92368OpenAlexW2098870701MaRDI QIDQ2263703FDOQ2263703
Authors: Shinsaku Fujita
Publication date: 19 March 2015
Published in: Journal of Mathematical Chemistry (Search for Journal in Brave)
Full work available at URL: https://doi.org/10.1007/s10910-014-0427-9
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Cites Work
- Integrated discussion on stereogenicity and chirality for restructuring stereochemistry
- 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
- Title not available (Why is that?)
- Three aspects of an absolute configuration on the basis of the stereoisogram approach and revised terminology on related stereochemical concepts
- Title not available (Why is that?)
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Cited In (14)
- Type-itemized enumeration of RS-stereoisomers of octahedral complexes
- Importance of the proligand-promolecule model in stereochemistry. II: The stereoisogram approach to stereoisomeric features of prismane derivatives
- Type-itemized enumeration of quadruplets of \textit{RS}-stereoisomers. I: Cycle indices with chirality fittingness modulated by type-IV quadruplets
- Type-itemized enumeration of quadruplets of \textit{RS}-stereoisomers. II: Cycle indices with chirality fittingness modulated by type-V quadruplets
- 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
- Three aspects of an absolute configuration on the basis of the stereoisogram approach and revised terminology on related stereochemical concepts
- Stereoisograms for specifying chirality and RS-stereogenicity. A versatile tool for avoiding the apparent inconsistency between geometrical features and RS-nomenclature in stereochemistry
- Stereoisograms for three-membered heterocycles. I: Symmetry-itemized enumeration of oxiranes under an \textit{RS}-stereoisomeric group
- Stereoisograms for three-membered heterocycles. III: \textit{R/S}-stereodescriptors for characterizing the \textit{RS}-stereogenic aspect of absolute configuration
- Correlation diagrams of stereoisograms for characterizing stereoisomers of cyclobutane deriva\-tives
- Stereoisograms for three-membered heterocycles. IV: Half-size-subgroup method for type-itemized enumeration of oxiranes under an \textit{RS}-stereoisomeric group
- Stereoisograms for three-membered heterocycles. V: Factor-group method for type-itemized enumeration of oxiranes under an \textit{RS}-stereoisomeric group
- Stereoisograms for three-membered heterocycles. V: Factor-group method for type-itemized enumeration of oxiranes under an \textit{RS}-stereoisomeric group
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