| dc.contributor.author | Kumar, Anil | |
| dc.date.accessioned | 2026-01-19T09:32:09Z | |
| dc.date.available | 2026-01-19T09:32:09Z | |
| dc.date.issued | 2025 | |
| dc.identifier.uri | https://pubs.acs.org/doi/full/10.1021/acs.orglett.5c02418 | |
| dc.identifier.uri | http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/20579 | |
| dc.description.abstract | A Ru(II)-catalyzed inherent weakly coordinating oxo-group-directed site-selective C5 functionalization of 2-arylquinolin-4(1H)-ones using various coupling partners like allyl alcohols, acrylates, styrenes, maleimides, and acrylamide has been described. The developed method allowed the synthesis of C5-substituted 2-arylquinolin-4(1H)-ones in good to excellent yields. The protocol is compatible with a broad range of functional groups and can be used on the gram scale. In addition, based on the control experiments, a plausible reaction mechanism has been proposed for this transformation. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | ACS | en_US |
| dc.subject | Chemistry | en_US |
| dc.subject | Ru(II) catalysis | en_US |
| dc.subject | C5 functionalization | en_US |
| dc.subject | Quinolinone derivatives | en_US |
| dc.subject | Site-selective coupling | en_US |
| dc.title | Inherent weakly coordinating oxo-group-directed ruthenium(ii)-catalyzed C5 functionalization of 2-arylquinolin-4(1h)-ones | en_US |
| dc.type | Article | en_US |
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