Department of Chemistry, Graduate School of Science and Technology, Kumamoto University, Kurokami 2-39-1, Kumamoto 860-8555, Japan
Department of Chemistry, Kumamoto University, Kurokami 2-39-1, Kumamoto 860-8555, Japan
Author to whom correspondence should be addressed.
Academic Editors: Luke R. Odell and Norbert Haider
Received: 7 September 2016 / Revised: 12 October 2016 / Accepted: 14 October 2016 / Published: 20 October 2016
The facile synthesis of 4-acetyl-2-hydroxy-2,5-dimethylfuran-3(2H
) was achieved by the Mn(OAc)3
-mediated aerobic oxidation of 2,4-pentanedione or the direct reaction of Mn(acac)3
in AcOH-TFE at room temperature under a dried air stream.
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MDPI and ACS Style
Akazaki, C.; Kawabata, S.; Nishino, H. 4-Acetyl-2-hydroxy-2,5-dimethylfuran-3(2H)-one. Molbank 2016, 2016, M913.
Akazaki C, Kawabata S, Nishino H. 4-Acetyl-2-hydroxy-2,5-dimethylfuran-3(2H)-one. Molbank. 2016; 2016(4):M913.
Akazaki, Chiaki; Kawabata, Shun; Nishino, Hiroshi. 2016. "4-Acetyl-2-hydroxy-2,5-dimethylfuran-3(2H)-one." Molbank 2016, no. 4: M913.
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