Publication: Convenient synthesis of α-nitrooximes mediated by OXONE®
| dc.contributor.author | Napasawan Chumnanvej | en_US |
| dc.contributor.author | Natthapol Samakkanad | en_US |
| dc.contributor.author | Manat Pohmakotr | en_US |
| dc.contributor.author | Vichai Reutrakul | en_US |
| dc.contributor.author | Thaworn Jaipetch | en_US |
| dc.contributor.author | Darunee Soorukram | en_US |
| dc.contributor.author | Chutima Kuhakarn | en_US |
| dc.contributor.other | Mahidol University | en_US |
| dc.date.accessioned | 2018-11-09T02:03:22Z | |
| dc.date.available | 2018-11-09T02:03:22Z | |
| dc.date.issued | 2014-01-01 | en_US |
| dc.description.abstract | © The Royal Society of Chemistry 2014. A novel OXONE® mediated direct difunctionalization of alkenes with NaNO<inf>2</inf> in aqueous acetonitrile for the synthesis of α-nitrooximes was developed. The α-nitrooximes were readily prepared in moderate to high yields at room temperature under mild reaction conditions. The present protocol offers an easy and environmentally benign approach to access various α-nitrooximes derived from styrene derivatives. | en_US |
| dc.identifier.citation | RSC Advances. Vol.4, No.104 (2014), 59726-59732 | en_US |
| dc.identifier.doi | 10.1039/c4ra11703d | en_US |
| dc.identifier.issn | 20462069 | en_US |
| dc.identifier.other | 2-s2.0-84912038846 | en_US |
| dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/33576 | |
| dc.rights | Mahidol University | en_US |
| dc.rights.holder | SCOPUS | en_US |
| dc.source.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84912038846&origin=inward | en_US |
| dc.subject | Chemical Engineering | en_US |
| dc.subject | Chemistry | en_US |
| dc.title | Convenient synthesis of α-nitrooximes mediated by OXONE® | en_US |
| dc.type | Article | en_US |
| dspace.entity.type | Publication | |
| mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84912038846&origin=inward | en_US |