397251-89-7Relevant academic research and scientific papers
Alcohol substitution and dehydrogenation of selenium compounds: A convenient preparation of trisubstituted furans from allyl-substituted 1,3-dicarbonyls
Tang,Huang, Xian
, p. 312 - 313 (2008)
Trisubstituted furans have been synthesised efficiently by an alcohol substitution and dehydrogenation reaction of selenocyclic enol ethers which were prepared by organoselenium-induced regioselective electrophilic intramolecular cyclisation of allyl-substituted 1,3-dicarbonyls.
Electrophilic cyclization of alkenyl β-dicarbonyl compounds: A comparative study
Ferraz, Helena M. C.,Nunes, Marta R. S.,Bianco, Graziela G.
, p. 153 - 158 (2001)
This work describes a comparative study between PhSeBr, ArTeCl3and I2 toward the electrophilic cyclization of some unsaturated β-keto esters and β-diketones. The oxidation/elimination reaction of the obtained selenides was also studi
Synthesis of cyclic enol ethers from alkenyl-β-dicarbonyl compounds
Ferraz, Helena M. C.,Sano, Myrian K.,Nunes, Marta R. S.,Bianco, Graziela G.
, p. 4122 - 4126 (2007/10/03)
In this work we describe the cyclofunctionalization of eleven differently substituted alkenyl-β-dicarbonyl compounds, employing three electrophilic reagents, namely, iodine, ρ-methoxyphenyl-tellurium trichloride, and phenylselenenyl bromide. The reactions occur through the enolic form of the substrates, to afford the corresponding iodo-, telluro-, or selenocyclic enol ethers. Substrates bearing trisubstituted double bonds failed in reacting with the selenium and tellurium reagents. In general, β-diketones reacted faster than β-keto esters with the three studied electrophiles.
