Publication: α-arylsulfanyl-α-fluoro carbenoids: Their novel chemistry and synthetic applications
| dc.contributor.author | Manat Pohmakotr | en_US |
| dc.contributor.author | Winai Ieawsuwan | en_US |
| dc.contributor.author | Patoomratana Tuchinda | en_US |
| dc.contributor.author | Palangpon Kongsaeree | en_US |
| dc.contributor.author | Samran Prabpai | en_US |
| dc.contributor.author | Vichai Reutrakul | en_US |
| dc.contributor.other | Mahidol University | en_US |
| dc.date.accessioned | 2018-07-24T03:36:00Z | |
| dc.date.available | 2018-07-24T03:36:00Z | |
| dc.date.issued | 2004-11-25 | en_US |
| dc.description.abstract | (Chemical equation presented) The bromine-magnesium exchange reactions of arylthiobromodifluoromethanes with Grignard reagents have been studied. Upon trapping with electrophiles, alkyl aryl sulfides and ketenedithioacetals are obtained. The reaction is proposed to occur via novel α-arylsulfanyl- α-fluoro carbenoids. The first examples of arylthiomethane multipole synthons are also reported. | en_US |
| dc.identifier.citation | Organic Letters. Vol.6, No.24 (2004), 4547-4550 | en_US |
| dc.identifier.doi | 10.1021/ol048085m | en_US |
| dc.identifier.issn | 15237060 | en_US |
| dc.identifier.other | 2-s2.0-10044224653 | en_US |
| dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/21117 | |
| 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=10044224653&origin=inward | en_US |
| dc.subject | Biochemistry, Genetics and Molecular Biology | en_US |
| dc.title | α-arylsulfanyl-α-fluoro carbenoids: Their novel chemistry and synthetic applications | en_US |
| dc.type | Article | en_US |
| dspace.entity.type | Publication | |
| mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=10044224653&origin=inward | en_US |