6268-56-0Relevant academic research and scientific papers
Lewis Acid-Promoted Disproportionation Reaction of Aromatic Vinyl Ethers and Acetals and Its Application to the Synthesis of Paracotoin
Gong, Young Dae,Tanaka, Hiroko,Iwasawa, Nobuharu,Narasaka, Koichi
, p. 2181 - 2185 (2007/10/03)
Aromatic vinyl ethers and acetals underwent a novel addition-fragmentation reaction affording olefins and esters in the presence of a Lewis acid. This reaction was applied to intramolecular cyclization reaction, giving five or six membered ring compounds in good yields. Paracotoin, an intermediate in the biosynthesis of shikimic acid, was synthesized using this cyclization reaction as the key step.
Synthesis and structure activity relationships of fibrinolytic 1,ω diphenyl 1,ω alkanediamines
Fliedner Jr,Myers,Schor,Pachter
, p. 749 - 754 (2007/10/06)
The promising results obtained in animal clot lysis experiments with the fibrinolytic bis(tetrahydroiso quinolines) VI prompted the preparation of a related series of 1,ω diphenyl 1,ω alkanediamines V. As measured in the standard rat screen (ip) the compo
