Prochirality and Pro-RS-Stereogenicity. Stereoisogram Approach Free from the Conventional “Prochirality” and “Prostereogenicity”-Reference-Cited by-同舟云学术

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Prochirality and Pro-RS-Stereogenicity. Stereoisogram Approach Free from the Conventional “Prochirality” and “Prostereogenicity”

Published:2011 Issue: Volume: Page:227-271
ISSN:1875-0745
Container-title:Carbon Bonding and Structures
language:
Short-container-title:

Author:

Fujita Shinsaku

Publisher

Springer Netherlands

Link

http://link.springer.com/content/pdf/10.1007/978-94-007-1733-6_10

Reference71 articles.

1. Black KA (1990) J Chem Educ 67:141–142

2. Cahn RS, Ingold CK, Prelog V (1966) Angew Chem Int Ed Engl 5:385– 415

3. Eliel EL (1982) Top Curr Chem 105:1–76

4. Eliel EL, Wilen SH (1994) Stereochemistry of organic compounds. Wiley, New York

5. Eliel EL, Willen SH, Doyle MP (2001) Basic organic stereochemistry. Wiley-Interscience, New York

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

2. 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

3. Asymmetry revisited by Fujita’s stereoisogram approach. Part 1: Asymmetry under point-group symmetry and under RS-permutation-group symmetry;Tetrahedron: Asymmetry;2016-08

4. Systematic Enumeration and Symmetries of Cubane Derivatives;The Chemical Record;2016-03-29

5. Symmetry-Itemized Enumeration of Quadruplets ofRS-Stereoisomers Derived from a Trigonal Pyramidal Skeleton;Bulletin of the Chemical Society of Japan;2015-09-15

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