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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 34, 2004 - Issue 23
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Original Articles

Ring Opening of 3‐Bromo‐2‐Isoxazolines to β‐Hydroxy Nitriles

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Pages 4387-4394 | Received 02 Aug 2004, Published online: 10 Jan 2011
 

Abstract

3‐Bromo‐2‐isoxazolines were converted to the corresponding β‐hydroxy nitriles by treatment with sodium iodide in the presence of either chlorotrimethylsilane or para‐toluenesulfonic acid. Both methods gave β‐hydroxy nitriles under relatively mild conditions in good to moderate yields for a variety of substituted 3‐bromo‐2‐isoxazolines.

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