Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,6-Lutidine | HCID 7937 | — |
| Reactant | p-Chlorophenacyl bromide | HCID 68303 | — |
| Reactant | Hept-6-ynal | HCID 11355455 | — |
| Catalyst | 5-Benzyl-2-tert-butyl-3-methyl-4-imidazolidinone, (2S,5S)- | HCID 10309834 | — |
| Catalyst | Tris(2,2-bipyridyl)ruthenium(II) chloride hexahydrate | HCID 16211607 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178444632 | HCID 178444632 | — |
| Product | HCID 178444633 | HCID 178444633 | — |
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-58351e3153d14c88b60ccf1b2278615e |
|---|
| Source note | Dataset from `Ultra-high-throughput mapping of the chemical space of asymmetric catalysis enables accelerated reaction discovery` |
|---|
