aza-oxyallyl cation intermediates with a variety of carbonyl compounds is reported to construct 4-oxazolidinones motifs with good yields and diastereoselectivities. This simple and efficient (3 + 2) cycloaddition method provides direct access to potential bioactive compounds.
据报道,原位生成的氮杂-氧基烯丙基阳离子中间体与各种羰基化合物的新型反应性可构建具有良好收率和非对映选择性的4-
恶唑烷酮基序。这种简单有效的(3 + 2)环加成方法可直接获得潜在的
生物活性化合物。