Publication: Friedel-crafts-type alkylation with bromodifluoro(phenylsulfanyl)methane through α-fluorocarbocations: Syntheses of thioesters, benzophenones and xanthones
| dc.contributor.author | Chutima Kuhakarn | en_US |
| dc.contributor.author | Nakin Surapanich | en_US |
| dc.contributor.author | Siriporn Kamtonwong | en_US |
| dc.contributor.author | Manat Pohmakotr | en_US |
| dc.contributor.author | Vichai Reutrakul | en_US |
| dc.contributor.other | Mahidol University | en_US |
| dc.date.accessioned | 2018-05-03T08:06:37Z | |
| dc.date.available | 2018-05-03T08:06:37Z | |
| dc.date.issued | 2011-10-01 | en_US |
| dc.description.abstract | Bromodifluoro(phenylsulfanyl)methane undergoes a Friedel-Crafts-type alkylation, through α-fluorocarbocations, with activated aromatic compounds yielding thioesters and/or benzophenones. The methodology has been applied to the synthesis of naturally occurring xanthone derivatives. © 2011 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim. | en_US |
| dc.identifier.citation | European Journal of Organic Chemistry. No.29 (2011), 5911-5918 | en_US |
| dc.identifier.doi | 10.1002/ejoc.201100715 | en_US |
| dc.identifier.issn | 10990690 | en_US |
| dc.identifier.issn | 1434193X | en_US |
| dc.identifier.other | 2-s2.0-80053963296 | en_US |
| dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/123456789/11691 | |
| 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=80053963296&origin=inward | en_US |
| dc.subject | Chemistry | en_US |
| dc.title | Friedel-crafts-type alkylation with bromodifluoro(phenylsulfanyl)methane through α-fluorocarbocations: Syntheses of thioesters, benzophenones and xanthones | en_US |
| dc.type | Article | en_US |
| dspace.entity.type | Publication | |
| mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=80053963296&origin=inward | en_US |