pro-R, pro-S
Term · Chemistry · MLC-T-CHM-009558
Stereodescriptors used to distinguish between two identical ligands on a prochiral center, typically a carbon atom, that if replaced by a different group, would lead to an R or S configuration, respectively. These designations are assigned according to the Cahn-Ingold-Prelog priority rules. For instance, in ethanol (CH3CH2OH), the two hydrogen atoms on the methylene carbon are pro-R and pro-S.
| Identifier | MLC-T-CHM-009558 |
|---|---|
| Field | Chemistry |
| Subject | Organic and Biomolecular Chemistry |
| References | PAC, 1996, 68, 2193. 'Basic terminology of stereochemistry (IUPAC Recommendations 1996)' on page 2214 (https://doi.org/10.1351/pac199668122193) |
| See also | CIP priority; Chiral; Prochirality; Prochirality centre; Stereodescriptor; Stereoheterotopic |
Record as JSON
{
"id": "MLC-T-CHM-009558",
"term": "pro-R, pro-S",
"field": "Chemistry",
"definition": "Stereodescriptors used to distinguish between two identical ligands on a prochiral center, typically a carbon atom, that if replaced by a different group, would lead to an R or S configuration, respectively. These designations are assigned according to the Cahn-Ingold-Prelog priority rules. For instance, in ethanol (CH3CH2OH), the two hydrogen atoms on the methylene carbon are pro-R and pro-S.",
"subject": "Organic and Biomolecular Chemistry",
"see_also": [
"CIP priority",
"chiral",
"prochirality",
"prochirality centre",
"stereodescriptor",
"stereoheterotopic"
],
"references": [
"PAC, 1996, 68, 2193. 'Basic terminology of stereochemistry (IUPAC Recommendations 1996)' on page 2214 (https://doi.org/10.1351/pac199668122193)"
],
"url": "https://mlchart.com/terminology/chemistry/pro-r-pro-s/"
}
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