作者:G. Desimoni、G. Minoli
DOI:10.1016/s0040-4020(01)98687-9
日期:1968.1
The synthesis of 3-phenyl-4,5-diaminoisoxazole from 3-phenyl-5-acetylaminoisoxazole in a three-step sequence has been described. The reaction of the diaminoisoxazole with several α-diketones represents a convenient route to isoxazolo [4.5-b] pyrazine derivatives.
已经描述了以三步顺序从3-苯基-5-乙酰基
氨基
异恶唑合成3-苯基-4,5-二
氨基
异恶唑。二
氨基
异恶唑与几种α-二酮的反应代表了制备
异恶唑啉[4.5-b]
吡嗪衍
生物的便捷途径。