1676-65-9Relevant academic research and scientific papers
Cyclization of 1-Aryl-5-Phenylpent-4-en-2-yn-1-Ones to 2,3-Dihydropyran-2-Ones in Trifluoromethanesulfonic Acid
Zalivatskaya, Anna S.,Golovanov, Aleksander А.,Vasilyev, Aleksander V.
, p. 953 - 956 (2020/08/26)
[Figure not available: see fulltext.] Under the action of an excess of trifluoromethanesulfonic acid, 1-aryl-5-phenylpent-4-en-2-yn-1-ones cyclize intramolecularly to 6-aryl-2-phenyl-2,3-dihydropyran-4-ones. The reaction proceeds at room temperature for 1
(Benzoyliodomethyl)triphenylphosphonium Iodide: A Convenient Reagent for Direct Synthesis of Arylethynyl Phenyl Ketones by Chain Extension of Aldehydes
Iman, Manoutcher,Bouyssou, Pascal,Chenault, Jacques
, p. 631 - 632 (2007/10/02)
Reaction between (benzoyliodomethyl)triphenylphosphonium iodide, potassium carbonate and various aromatic aldehydes in a liquid-solid two-phase system, gives arylethynyl phenyl ketones in good yield.
