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Easy Access to Evans’ Oxazolidinones. Stereoselective Synthesis and Antibacterial Activity of a New 2-Oxazolidinone Derivative

机译:轻松获得Evans的恶唑烷酮。新型2-Oxazolidinone衍生物的立体选择性合成和抗菌活性

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摘要

An interesting new approach was developed for the synthesis of Evans’ chiral auxiliaries with excellent yields. In turn, another new stereoselective and efficient strategy has also allowed for the preparation of a 2-oxazolidinone derivative in 34% overall yield from the Morita-Baylis-Hillman adduct. The antibacterial activity of this oxazolidinone was tested against Staphylococcus aureus strains isolated from animals with mastitis infections.
机译:开发了一种有趣的新方法,用于合成埃文斯手性助剂,具有优异的收率。反过来,另一种新的立体选择性和有效的策略也允许由森田-贝利斯-希尔曼加合物制备总收率为34%的2-恶唑烷酮衍生物。测试了该恶唑烷酮对分离自患有乳腺炎感染动物的金黄色葡萄球菌菌株的抗菌活性。

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