Three aspects of an absolute configuration on the basis of the stereoisogram approach and revised terminology on related stereochemical concepts
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Publication:460905
DOI10.1007/S10910-014-0326-0zbMATH Open1296.92241OpenAlexW2063679534MaRDI QIDQ460905FDOQ460905
Authors: Shinsaku Fujita 
Publication date: 9 October 2014
Published in: Journal of Mathematical Chemistry (Search for Journal in Brave)
Full work available at URL: https://doi.org/10.1007/s10910-014-0326-0
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stereoisogram\(RS\)-stereodescriptor\(RS\)-stereoisomeric groupabsolute configurationchirality faithfulness
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
- Symmetry and combinatorial enumeration in chemistry.
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- 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
- Itemized enumeration of quadruplets of RS-stereoisomers under the action of RS-stereoisomer\-ic groups
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Cited In (7)
- Importance of the proligand-promolecule model in stereochemistry. II: The stereoisogram approach to stereoisomeric features of prismane derivatives
- Hierarchical enumeration of octahedral complexes by using combined-permutation representations
- 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
- Stereogenicity/astereogenicity as global/local permutation-group symmetry and relevant concepts for restructuring stereochemistry
- 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
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