620-97-3Relevant academic research and scientific papers
Synthesis of 6-substituted 3-(alkoxycarbonyl)-5-aryl-α-pyrones
Miura, Takuya,Fujioka, Saki,Takemura, Naoto,Iwasaki, Hiroki,Ozeki, Minoru,Kojima, Naoto,Yamashita, Masayuki
, p. 496 - 502 (2014/03/21)
An efficient synthesis of 6-substituted 3-(alkoxycarbonyl)-5-aryl-α- pyrones is reported. This methodology consists of the successive manipulation of an addition-elimination reaction between benzyl ketone derivatives and dimethyl methoxymethylenemalonate,
Electroreductive Acylation of Benzyl Chlorides with Acid Anhydrides. Stereoselective Formation of (E)-Enol Esters from Benzyl Alkyl Ketones
Nishiguchi, Ikuzo,Oki, Tsuneo,Hirashima, Tsuneaki,Shiokawa, Jiro
, p. 2005 - 2008 (2007/10/02)
Electroreduction of benzyl chlorides in the presence of acid anhydrides brought about stereoselective formation of (E)-enol esters of the corresponding benzyl alkyl ketones, the initial acylated products, in good to moderate yields.
