Group-theoretical Foundations for the Concept of Mandalas as Diagrammatical Expressions for Characterizing Symmetries of Stereoisomers-Reference-Cited by-同舟云学术

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Group-theoretical Foundations for the Concept of Mandalas as Diagrammatical Expressions for Characterizing Symmetries of Stereoisomers

Published:2006-06-13 Issue:3 Volume:42 Page:481-534
ISSN:0259-9791
Container-title:Journal of Mathematical Chemistry
language:en
Short-container-title:J Math Chem

Author:

Fujita Shinsaku

Publisher

Springer Science and Business Media LLC

Subject

Applied Mathematics,General Chemistry

Link

http://link.springer.com/content/pdf/10.1007/s10910-006-9128-3.pdf

Reference37 articles.

1. Mislow K., Raban M. (1967) Top. Stereochem. 1: 1–38

2. Eliel E.L. (1980) J. Chem. Educ. 57: 52–55

3. Mislow K., Siegel J. (1984) J. Am. Chem. Soc. 106: 3319–3328

4. Eliel E., Wilen S.H. (1994). Stereochemistry of Organic Compounds. Wiley, New York

5. North N. (1998). Principles and Applications of Stereochemistry. Stanley Thornes, Cheltenham

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1. Symmetry-itemized enumeration of RS-stereoisomers of allenes. I. The fixed-point matrix method of the USCI approach combined with the stereoisogram approach;Journal of Mathematical Chemistry;2014-03-11

2. Prochirality and Pro-RS-Stereogenicity. Stereoisogram Approach Free from the Conventional “Prochirality” and “Prostereogenicity”;Carbon Bonding and Structures;2011

3. Numbers of Alkanes and Monosubstituted Alkanes. A Long-Standing Interdisciplinary Problem over 130 Years;Bulletin of the Chemical Society of Japan;2010-01-15

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