Stereoisograms of trigonal bipyramidal compounds. I: Chirality and RS-stereogenicity free from the conventional ``chirality and ``stereogenicity
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Publication:445405
DOI10.1007/S10910-012-0006-XzbMATH Open1314.92180OpenAlexW2050798058MaRDI QIDQ445405FDOQ445405
Publication date: 24 August 2012
Published in: Journal of Mathematical Chemistry (Search for Journal in Brave)
Full work available at URL: https://doi.org/10.1007/s10910-012-0006-x
stereoisogram\(C\)/\(A\)-descriptor\(RS\)-diastereomericinorganic stereochemistrytrigonal bipyramidal compound
Cites Work
- Integrated discussion on stereogenicity and chirality for restructuring stereochemistry
- Title not available (Why is that?)
- Stereogenicity/astereogenicity as global/local permutation-group symmetry and relevant concepts for restructuring stereochemistry
- Correlation diagrams of stereoisograms for characterizing stereoisomers of cyclobutane deriva\-tives
Cited In (1)
Recommendations
- Stereoisograms of trigonal bipyramidal compounds. II: \(RS\)-stereogenicity/\(RS\)-stereoisomerism versus stereogenicity/stereoisomerism, leading to a revised interpretation of Berry's pseudorotation π π
- Stereoisograms for three-membered heterocycles. II: Chirality, \textit{RS}-stereogenicity, and \textit{ortho}-stereogenicity on the basis of the proligand-promolecule model π π
- Three aspects of an absolute configuration on the basis of the stereoisogram approach and revised terminology on related stereochemical concepts π π
- Stereoisograms for three-membered heterocycles. III: \textit{R/S}-stereodescriptors for characterizing the \textit{RS}-stereogenic aspect of absolute configuration π π
- Importance of the proligand-promolecule model in stereochemistry. II: The stereoisogram approach to stereoisomeric features of prismane derivatives π π
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