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cycles per second cyclitols

cyclic acid anhydrides (cyclic anhydrides)

Acid anhydrides derived by loss of water between two oxoacid functions RkE(=O)l(OH)m (l ≠ 0) (carboxylic, sulfonic, etc.) in the same molecule so as to close a ring. Oxo oxygen replacement analogues are included, e.g.
C01492
See: thioanhydrides
Source:
PAC, 1995, 67, 1307 (Glossary of class names of organic compounds and reactivity intermediates based on structure (IUPAC Recommendations 1995)) on page 1329
InChI=1/C7H4O3S2/c8-12(9)6-4-2-1-3-5(6)7(11)10-12/h1-4H
TUQVVSJURGXDNC-UHFFFAOYAT
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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.C01492.
Original PDF version: http://www.iupac.org/goldbook/C01492.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 The PDF version is out of date and is provided for reference purposes only.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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