Stereoisograms for reorganizing the theoretical foundations of stereochemistry and stereoisomerism. Part 3: rational avoidance of misleading standpoints for pro-R/pro-S-descriptors-Reference-Cited by-同舟云学术

Stereoisograms for reorganizing the theoretical foundations of stereochemistry and stereoisomerism. Part 3: rational avoidance of misleading standpoints for pro-R/pro-S-descriptors

Published:2014-09 Issue:16-17 Volume:25 Page:1190-1204
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Fujita Shinsaku

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference31 articles.

1. Specification of Molecular Chirality

2. Basic Principles of the CIP-System and Proposals for a Revision

3. IUPAC Chemical Nomenclature and Structure Representation Division. Provisional Recommendations. Nomenclature of Organic Chemistry 2004. http://www.iupac.org/reports/provisional/abstract04/favre_310305.html.

4. Applications of the Sequence Rule. I. Naming the Paired Ligands g,g at a Tetrahedral Atom Xggij. II. Naming the Two Faces of a Trigonal Atom Yghi

5. Prochiral and pseudoasymmetric centers: Implications of recent definitions

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1. Type-Itemized Enumeration of Five Types of Stereoisograms and Their Simplified Diagrams for Characterizing Cubane Derivatives;Bulletin of the Chemical Society of Japan;2022-03-15

2. Pseudoasymmetry paradox: A suggestion to introduce the term pseudostereogenicity and address reflection issues;Tetrahedron;2020-06

3. Conceptual defects of modern stereochemistry. Comprehensive remedy by stereoisograms based on RS-stereoisomerism for mediating between enantiomerism and stereoisomerism;Tetrahedron: Asymmetry;2017-01

4. Mathematical Stereochemistry as the Theoretical Foundations of Organic and Inorganic Chemistry;Journal of Computer Chemistry, Japan;2017

5. Chirality andRS-Stereogenicity as Two Kinds of Handedness. Their Aufheben by Fujita’s Stereoisogram Approach for Giving New Insights into Classification of Isomers;Bulletin of the Chemical Society of Japan;2016-09-15