Publication: Fluoromethyl phenyl sulfoxide: Highly convenient syntheses of vinyl fluorides and fluoromethylketones
dc.contributor.author | Vichai Reutrakul | en_US |
dc.contributor.author | Vatcharin Rukachaisirikul | en_US |
dc.contributor.other | Mahidol University | en_US |
dc.date.accessioned | 2018-10-12T07:34:05Z | |
dc.date.available | 2018-10-12T07:34:05Z | |
dc.date.issued | 1983-01-01 | en_US |
dc.description.abstract | Alkylation of lithio fluoromethyl phenyl sulfoxide 2 gave the alkylated products in high yields. Pyrolysis of the products led to vinyl fluorides in excellent yields. The reaction of 2 with carbonyl compounds led to the corresponding β-hydroxy-α-fluoromethyl phenyl sulfoxides. Pyrolysis of some of the sulfoxides gave fluoromethylketones in moderate yields. © 1983. | en_US |
dc.identifier.citation | Tetrahedron Letters. Vol.24, No.7 (1983), 725-728 | en_US |
dc.identifier.doi | 10.1016/S0040-4039(00)81509-9 | en_US |
dc.identifier.issn | 00404039 | en_US |
dc.identifier.other | 2-s2.0-0000086269 | en_US |
dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/30447 | |
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=0000086269&origin=inward | en_US |
dc.subject | Biochemistry, Genetics and Molecular Biology | en_US |
dc.subject | Chemistry | en_US |
dc.subject | Pharmacology, Toxicology and Pharmaceutics | en_US |
dc.title | Fluoromethyl phenyl sulfoxide: Highly convenient syntheses of vinyl fluorides and fluoromethylketones | en_US |
dc.type | Article | en_US |
dspace.entity.type | Publication | |
mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0000086269&origin=inward | en_US |