Di-and Tri-2-furoylmethane
GS Hammond, FS Schultz
Index: Hammond; Schultz Journal of the American Chemical Society, 1952 , vol. 74, p. 329,331
Full Text: HTML
Citation Number: 2
Abstract
Di-and tri-2-furoylmethane have been identified as by-products in the synthesis of 2- acetylfuran by the reaction of furoyl chloride with dimethylcadmium. The compounds have also been prepared by conventional synthetic procedures. The near ultraviolet absorption spectra of the new ketones indicate that both are highly enolized in ethanol solutions. The spectra of the enolate anions are strikingly similar to those of the enols. This appears to be ...
Related Articles:
Structure and reactivity of bis (iodozincio) methane solution
[Matsubara, Seijiro; Yoshino, Hideaki; Yamamoto, Yuhei; Oshima, Koichiro; Matsuoka, Hideki; Matsumoto, Kozo; Ishikawa, Kazuhiko; Matsubara, Eiichiro Journal of Organometallic Chemistry, 2005 , vol. 690, # 24-25 p. 5546 - 5551]
[Nomura, Kenichi; Asano, Keisuke; Kurahashi, Takuya; Matsubara, Seijiro Heterocycles, 2008 , vol. 76, # 2 p. 1381 - 1399]
Structure and Reactivity of Bis (iodozincio) methane in Tetrahydrothiophene
[Matsubara, Seijiro; Yamamoto, Yuhei; Utimoto, Kiitiro Synlett, 1999 , # 9 p. 1471 - 1473]
Acyl Exchanges between Esters and 1, 3-Diketones and β-Keto-esters
[McElvain; Weber Journal of the American Chemical Society, 1941 , vol. 63, p. 2192,2193]