This website uses cookies to give you the best user experience. If you continue
without changing your settings we'll assume you are happy to receive all RSC cookies.
You can change your cookie settings by navigating to our Privacy and Cookies page and following the instructions. These instructions
are also obtainable from the privacy link at the bottom of any RSC page.
Direct construction of 5-methyl-2-phenylisoxazol-3(2H)-ones via hypervalent iodine mediated sequential tandem oxidative cyclization of 3-oxo-N-phenylbutanamides catalyzed by zinc oxide (ZnO)
School of Chemistry and Life Science, Guangdong University of Petrochemical Technology, 139 of Guangdu Two Road, Maoming 525000, P. R. China
E-mail: lwb409@yahoo.com.cn
; Fax: +86-668-2923575
; Tel: +86-668-2923956
b
School of Pharmaceutical Sciences, Southern Medical University, Guangzhou 510515, China
E-mail: zzb24@yahoo.com.cn
Org. Biomol. Chem., 2013,11, 542-544
DOI:
10.1039/C2OB27145A
Received
04 Nov 2012,
Accepted
22 Nov 2012
First published online
26 Nov 2012
A sequential oxidative tandem cyclization reaction mediated by a combination of (diacetoxyiodo)benzene (DIB) with zinc oxide (ZnO) is presented for the synthesis of 5-methyl-2-phenylisoxazol-3(2H)-ones from β-ketobutylanilides. A variety of β-ketobutylanilide compounds were used in this approach, and a wide range of functionalized 5-methylisoxazol-3(2H)-ones were obtained in good to excellent yields.
Fetching data from CrossRef. This may take some time to load.
Organic & Biomolecular Chemistry
- Information Point