Ring Opening of 3‐Bromo‐2‐Isoxazolines to β‐Hydroxy Nitriles
摘要:
3-Bromo-2-isoxazolines were converted to the corresponding beta-hydroxy nitriles by treatment with sodium iodide in the presence of either chlorotrimethylsilane or para-toluenesulfonic acid. Both methods gave beta-hydroxy nitriles under relatively mild conditions in good to moderate yields for a variety of substituted 3-bromo-2-isoxazolines.
Ring Opening of 3‐Bromo‐2‐Isoxazolines to β‐Hydroxy Nitriles
作者:Martin G. Kociolek、Kyle P. Kalbarczyk
DOI:10.1081/scc-200039452
日期:2004.12.31
3-Bromo-2-isoxazolines were converted to the corresponding beta-hydroxy nitriles by treatment with sodium iodide in the presence of either chlorotrimethylsilane or para-toluenesulfonic acid. Both methods gave beta-hydroxy nitriles under relatively mild conditions in good to moderate yields for a variety of substituted 3-bromo-2-isoxazolines.