HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1813630Generated: October 30, 2026
4-Bromophenacyl bromide → HCID 178444622, compound
https://huagongshe.com/reaction/1813630
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Bromophenacyl bromide | HCID 7454 | — |
| Reactant | 2,6-Lutidine | HCID 7937 | — |
| Reactant | Hept-6-ynal | HCID 11355455 | — |
| Catalyst | Tris(2,2-bipyridyl)ruthenium(II) chloride hexahydrate | HCID 16211607 | — |
| Catalyst | (R)-alpha,alpha-Bis(3,5-bis(trifluoromethyl)phenyl)-2-pyrrolidinemethanol trimethylsilyl ether | HCID 16218311 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178444622 | HCID 178444622 | — |
| Product | HCID 178444623 | HCID 178444623 | — |
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` |
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| ORD ID | ord-52f42397eb934ab184dbf8d748fb37f4 |
|---|
| Source note | Dataset from `Ultra-high-throughput mapping of the chemical space of asymmetric catalysis enables accelerated reaction discovery` |
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