New Description of Molecular Chirality and Its Application to the Prediction of the Preferred Enantiomer in Stereoselective Reactions-Reference-Cited by-同舟云学术

New Description of Molecular Chirality and Its Application to the Prediction of the Preferred Enantiomer in Stereoselective Reactions

Published:2001-02-23 Issue:2 Volume:41 Page:369-375
ISSN:0095-2338
Container-title:Journal of Chemical Information and Computer Sciences
language:en
Short-container-title:J. Chem. Inf. Comput. Sci.

Author:

Aires-de-Sousa João¹,Gasteiger Johann¹

Affiliation:

1. Secção de Química Orgânica Aplicada, Departamento de Química, Centro de Química Fina e Biotecnologia, campus Faculdade de Ciências e Tecnologia, Universidade Nova de Lisboa, Quinta da Torre, 2825-114 Monte de Caparica, Portugal, and Computer-Chemie-Centrum, Institute for Organic Chemistry, University of Erlangen-Nürnberg, Nägelsbachstrasse 25, D-91052 Erlangen, Germany

Publisher

American Chemical Society (ACS)

Subject

Computational Theory and Mathematics,Computer Science Applications,Information Systems,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ci000125n

Reference30 articles.

1. Avnir, D.; Hel-Or, H. Z.; Mezey, P. G. Symmetry and Chirality: Continuous Measures. InThe Encyclopedia of Computational Chemistry; Schleyer, P. v. R., Allinger, N. L., Clark, T., Gasteiger, J., Kollman, P. A., Schaefer, H. F., III, Schreiner, P. R., Eds.; John Wiley & Sons: Chichester, U.K., 1998; Vol. 4, pp 2890−2901.

2. Continuous Symmetry Measures. 4. Chirality

3. Algebraic aspects of the chirality phenomenon in chemistry

4. Topological Organic Chemistry. 9. Graph Theory and Molecular Topological Indices of Stereoisomeric Organic Compounds

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