Graphical representation of stereochemical configuration (IUPAC Recommendations 2006)
@article{Brecher2006GraphicalRO, title={Graphical representation of stereochemical configuration (IUPAC Recommendations 2006)}, author={J. Brecher}, journal={Pure and Applied Chemistry}, year={2006}, volume={78}, pages={1897 - 1970} }
Abstract Stereochemical configuration is determined by the relationship of atoms in three-dimensional space, yet remains most commonly represented in two-dimensional media such as printed publications or computer screens. Recommendations are provided for the display of three-dimensional stereochemical information in two-dimensional diagrams in ways that avoid ambiguity and are likely to be understood correctly by all viewers. Examples are provided for all types of stereochemical configuration…
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References
SHOWING 1-10 OF 19 REFERENCES
Stereochemistry of Organic Compounds
- Chemistry
- 1962
Structure Stereoisomers Symmetry Configuration Properties of Stereoisomers: Stereoisomer Discrimination Separation of Stereoisomers, Resolution, Racemization Heterotopic Ligands and Faces…
Nomenclature of retinoids: recommendations 1981. IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN).
- ChemistryArchives of biochemistry and biophysics
- 1983
A panel of experts appointed to review the problem and make recommendations are presented here as recommendations that have been approved by IUPAC and IUB.
M.C. Escher: His Life and Complete Graphic Work: With a Fully Illustrated Catalogue
- Art
- 1982
Traces the life of the Dutch graphic artist and shows his enigmatic woodcuts and prints, fantasy landscapes, and intricate geometric designs.
IUPAC COMMISSION ON NOMENCLATURE OF ORGANIC CHEMISTRY*: RULES FOR THE NOMENCLATURE OF ORGANIC CHEMISTRY
- Chemistry
- 1976
Adv. Carbohydr. Chem. Biochem
- Adv. Carbohydr. Chem. Biochem
- 1955
J. Chem. Inf. Comput. Sci
- J. Chem. Inf. Comput. Sci
- 2002
See, for example, Figs. 10a and 11b in H. Maehr
- J. Chem. Inf. Comput. Sci
- 2002
Joint Commission on Biochemical Nomenclature; (b) IUPAC-IUBMB Joint Commission on Biochemical Nomenclature
- c) IUPAC-IUBMB Joint Commission on Biochemical Nomenclatured) IUPAC-IUBMB Joint Commission on Biochemical Nomenclature
- 1996