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

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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