Metal- and photocatalyst-free approach to visible-light-induced acylation of quinoxalinones
| dc.contributor.author | Niwetmarin W. | |
| dc.contributor.author | Saesian N. | |
| dc.contributor.author | Saruengkhanphasit R. | |
| dc.contributor.author | Eurtivong C. | |
| dc.contributor.author | Thasana N. | |
| dc.contributor.author | Ruchirawat S. | |
| dc.contributor.correspondence | Niwetmarin W. | |
| dc.contributor.other | Mahidol University | |
| dc.date.accessioned | 2024-05-17T18:13:21Z | |
| dc.date.available | 2024-05-17T18:13:21Z | |
| dc.date.issued | 2024-01-01 | |
| dc.description.abstract | A transition-metal- and photocatalyst-free photochemical reaction was successfully developed for the direct acylation of quinoxalin-2(1H)-ones, which was enabled by the formation of electron donor-acceptor (EDA) complexes. The use of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) as the electron donor allows efficient and operationally simple access to a series of C3-aroylated and acylated quinoxalin-2(1H)-ones with moderate to good yields. | |
| dc.identifier.citation | Organic and Biomolecular Chemistry (2024) | |
| dc.identifier.doi | 10.1039/d4ob00630e | |
| dc.identifier.issn | 14770520 | |
| dc.identifier.scopus | 2-s2.0-85192480079 | |
| dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/98351 | |
| dc.rights.holder | SCOPUS | |
| dc.subject | Chemistry | |
| dc.subject | Biochemistry, Genetics and Molecular Biology | |
| dc.title | Metal- and photocatalyst-free approach to visible-light-induced acylation of quinoxalinones | |
| dc.type | Article | |
| mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85192480079&origin=inward | |
| oaire.citation.title | Organic and Biomolecular Chemistry | |
| oairecerif.author.affiliation | Laboratory of Medicinal Chemistry | |
| oairecerif.author.affiliation | Chulabhorn Graduate Institute | |
| oairecerif.author.affiliation | Mahidol University | |
| oairecerif.author.affiliation | MHESI |