An efficient entry to 1,2-benzisoxazoles via1,3-dipolar cycloaddition of in situ generated nitrile oxides and benzyne†
Abstract
An efficient protocol for the synthesis of a range of 1,2-benzisoxazoles using an improved
* Corresponding authors
a
School of Chemistry, University of Nottingham, University Park, Nottingham, UK
E-mail:
john.moses@nottingham.ac.uk
Web: http://www.moseslabs.com
Fax: + 44 (0)115 951 3533
Tel: + 44 (0)115 951 3533
b GlaxoSmithKline, Research Medicines Centre, Stevenage, UK
An efficient protocol for the synthesis of a range of 1,2-benzisoxazoles using an improved
C. Spiteri, C. Mason, F. Zhang, D. J. Ritson, P. Sharma, S. Keeling and J. E. Moses, Org. Biomol. Chem., 2010, 8, 2537 DOI: 10.1039/B927235F
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