Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,6-Lutidine | HCID 7937 | — |
| Reactant | 2-Bromo-4'-methylacetophenone | HCID 69272 | — |
| Reactant | Hept-6-ynal | HCID 11355455 | — |
| Catalyst | Riboflavine tetrabutyrate | HCID 5065 | — |
| Catalyst | D-Proline | HCID 8988 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178444628 | HCID 178444628 | — |
| Product | HCID 178444629 | HCID 178444629 | — |
Provenance & Evidence
| DOI | 10.1038/s41467-023-42446-5 |
|---|
| Source dataset | Dataset from `Ultra-high-throughput mapping of the chemical space of asymmetric catalysis enables accelerated reaction discovery` |
|---|
| ORD ID | ord-404cc5cd2d504c57ace3266e4e2d6bde |
|---|
| Source note | Dataset from `Ultra-high-throughput mapping of the chemical space of asymmetric catalysis enables accelerated reaction discovery` |
|---|
