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• W2095355340 abstract "A series of novel oxazolidinone antibiotics having [2.2.1] and [2.2.2] bicyclic oxazine moieties at the C-5 side chain of the A-ring was synthesized by nitroso Diels-Alder reactions, from three linezolid analogs containing morpholine, piperazine and thiomorpholine, respectively, as the C-ring components. Subsequent N-O bond cleavage generated oxazolidinones with 4-amino cyclo-2-en-1-ol substituents. The in vitro antibacterial activities of these oxazolidinone analogs were evaluated." @default.
• W2095355340 created "2016-06-24" @default.
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• W2095355340 date "2010-02-01" @default.
• W2095355340 modified "2023-10-16" @default.
• W2095355340 title "Syntheses and antibacterial activity studies of new oxazolidinones from nitroso Diels–Alder chemistry" @default.
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• W2095355340 doi "https://doi.org/10.1016/j.bmcl.2009.10.018" @default.
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