In this microreview, the application of [3+2] cycloaddition reactions for the selective preparation of nitroisoxazoles and their hydrogenated analogs was analyzed on the basis of recent publications. It was found that most discussed processes are realized at room temperature with high or full selectivity.

中文翻译：

---

[3+2]环加成反应合成硝基异恶唑及其氢化类似物的最新进展（微评）

在这篇微综述中，根据最近发表的文献，分析了[3+2]环加成反应在选择性制备硝基异恶唑及其氢化类似物中的应用。研究发现，大多数讨论的过程都是在室温下实现的，具有高选择性或完全选择性。