Osones
Term · Chemistry · MLC-T-CHM-008355
An obsolescent name for 1,2-dicarbonyl sugar derivatives (1,2-ketoaldoses) with an aldehyde group at C-1 and a ketone group at C-2. Osones are usually prepared by hydrolysis of osazones, the sugar bis(phenylhydrazones), so they are products rather than intermediates of osazone formation. Reduction of an osone gives the 2-ketose, for example D-glucosone gives D-fructose.
| Identifier | MLC-T-CHM-008355 |
|---|---|
| Field | Chemistry |
| Subject | Organic and Biomolecular Chemistry |
| References | PAC, 1995, 67, 1307. 'Glossary of class names of organic compounds and reactivity intermediates based on structure (IUPAC Recommendations 1995)' on page 1354 (https://doi.org/10.1351/pac199567081307); White Book, 2nd ed., p. 132 (https://iupac.qmul.ac.uk/bibliog/white.html) |
| See also | Hydrolysis; Ketoaldoses; Osazones |
Record as JSON
{
"id": "MLC-T-CHM-008355",
"term": "Osones",
"field": "Chemistry",
"definition": "An obsolescent name for 1,2-dicarbonyl sugar derivatives (1,2-ketoaldoses) with an aldehyde group at C-1 and a ketone group at C-2. Osones are usually prepared by hydrolysis of osazones, the sugar bis(phenylhydrazones), so they are products rather than intermediates of osazone formation. Reduction of an osone gives the 2-ketose, for example D-glucosone gives D-fructose.",
"subject": "Organic and Biomolecular Chemistry",
"see_also": [
"hydrolysis",
"ketoaldoses",
"osazones"
],
"references": [
"PAC, 1995, 67, 1307. 'Glossary of class names of organic compounds and reactivity intermediates based on structure (IUPAC Recommendations 1995)' on page 1354 (https://doi.org/10.1351/pac199567081307)",
"White Book, 2nd ed., p. 132 (https://iupac.qmul.ac.uk/bibliog/white.html)"
],
"url": "https://mlchart.com/terminology/chemistry/osones/"
}
Record 8,878 of 13,676 in Chemistry terminology (MLC-0109). Request the full dataset.