Spiteri, Christian, Mason, Christopher, Zhang, Fengzhi , Ritson, Dougal J., Sharma, Pallavi, Keeling, Steve and Moses, John E. (2010) An efficient entry to 1,2-benzisoxazoles via 1,3-dipolar cycloaddition of in situ generated nitrile oxides and benzyne. Organic and Biomolecular Chemistry Articles, 8 (11). pp. 2537-2542. ISSN 1477-0520
Full content URL: http://pubs.rsc.org/en/content/articlelanding/2010...
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| Item Type: | Article |
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| Item Status: | Live Archive |
Abstract
An efficient protocol for the synthesis of a range of 1,2-benzisoxazoles using an improved 1,3-dipolar cycloaddition of nitrile oxides and benzyne is described. Key to the procedure is the in situ generation of the reactive nitrile oxide and benzyne reactants simultaneously.
| Additional Information: | An efficient protocol for the synthesis of a range of 1,2-benzisoxazoles using an improved 1,3-dipolar cycloaddition of nitrile oxides and benzyne is described. Key to the procedure is the in situ generation of the reactive nitrile oxide and benzyne reactants simultaneously. |
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| Keywords: | Benzisoxazole, benzyne, 1, 3-dipolar cycloaddition |
| Subjects: | F Physical Sciences > F160 Organic Chemistry |
| Divisions: | College of Science > School of Life Sciences |
| ID Code: | 7108 |
| Deposited On: | 21 Dec 2012 14:49 |
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