Publication:
A novel method for the synthesis of α-fluoroketones via Claisen rearrangement

Simple item page
dc.contributor.authorVichai Reutrakulen_US
dc.contributor.authorThongchai Kruahongen_US
dc.contributor.authorManat Pohmakotren_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-02-27T04:25:24Z
dc.date.available2018-02-27T04:25:24Z
dc.date.issued1994-07-04en_US
dc.description.abstractFluorine-facilitated Claisen rearrangement has been employed as a key step in the synthesis of α-fluoroketones 5. The elimination of sulfenic acid from the allyl ethers 3 are effected under FVP conditions. © 1994.en_US
dc.identifier.citationTetrahedron Letters. Vol.35, No.27 (1994), 4853-4856en_US
dc.identifier.doi10.1016/S0040-4039(00)76986-3en_US
dc.identifier.issn00404039en_US
dc.identifier.other2-s2.0-0028302433en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/9507
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0028302433&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleA novel method for the synthesis of α-fluoroketones via Claisen rearrangementen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0028302433&origin=inwarden_US

Files

Collections

Scopus 1991-2000