Prochirality
Term · Chemistry · MLC-T-CHM-009495
A geometric property of an achiral molecule or center that can be converted into a chiral one in a single substitution or addition step. An achiral trigonal planar center with three different attached groups is prochiral because adding a new group creates a chiral tetrahedral center. The two faces of the planar structure are designated 'Re' and 'Si' based on the Cahn-Ingold-Prelog priority rules of the attached groups.
| Identifier | MLC-T-CHM-009495 |
|---|---|
| Field | Chemistry |
| Subject | Organic and Biomolecular Chemistry |
| References | PAC, 1996, 68, 2193. 'Basic terminology of stereochemistry (IUPAC Recommendations 1996)' on page 2213 (https://doi.org/10.1351/pac199668122193) |
| See also | Chiral; Chirality centre; Desymmetrization; Diastereoisomerism; Diastereotopic; Enantiotopic; Stereoheterotopic |
Record as JSON
{
"id": "MLC-T-CHM-009495",
"term": "Prochirality",
"field": "Chemistry",
"definition": "A geometric property of an achiral molecule or center that can be converted into a chiral one in a single substitution or addition step. An achiral trigonal planar center with three different attached groups is prochiral because adding a new group creates a chiral tetrahedral center. The two faces of the planar structure are designated 'Re' and 'Si' based on the Cahn-Ingold-Prelog priority rules of the attached groups.",
"subject": "Organic and Biomolecular Chemistry",
"see_also": [
"chiral",
"chirality centre",
"desymmetrization",
"diastereoisomerism",
"diastereotopic",
"enantiotopic",
"stereoheterotopic"
],
"references": [
"PAC, 1996, 68, 2193. 'Basic terminology of stereochemistry (IUPAC Recommendations 1996)' on page 2213 (https://doi.org/10.1351/pac199668122193)"
],
"url": "https://mlchart.com/terminology/chemistry/prochirality/"
}
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