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erythro, threo

Descriptors of the diastereoisomers of an acyclic structure or partial structure having two stereogenic centres. This notation is derived from carbohydrate nomenclature. The extension of this system has given rise to conflicting interpretations of these prefixes. It is recommended that for such cases the l,u or R *, S * system should be used.
Source:
PAC, 1996, 68, 2193 (Basic terminology of stereochemistry (IUPAC Recommendations 1996)) on page 2208
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IUPAC. Compendium of Chemical Terminology, 2nd ed. (the "Gold Book"). Compiled by A. D. McNaught and A. Wilkinson. Blackwell Scientific Publications, Oxford (1997). XML on-line corrected version: http://goldbook.iupac.org (2006-) created by M. Nic, J. Jirat, B. Kosata; updates compiled by A. Jenkins. ISBN 0-9678550-9-8. https://doi.org/10.1351/goldbook.
Last update: 2014-02-24; version: 2.3.3.
DOI of this term: https://doi.org/10.1351/goldbook.E02212.
Original PDF version: http://www.iupac.org/goldbook/E02212.pdf. The PDF version is out of date and is provided for reference purposes only. For some entries, the PDF version may be unavailable.
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