The synthesis and antibacterial activity of 1,3,4-Thiadiazole phenyl oxazolidinone analogues
Replacement of the morpholine C-ring of linezolid 1 with a 1,3,4-thiadiazolyl ring leads to oxazolidinone analogues 5 having potent antibacterial activity against both gram-positive and gram-negative organisms. Conversion of the C5 acetamide group to a thioacetamide further increases the potency of...
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Veröffentlicht in: | Bioorganic & medicinal chemistry letters 2003-12, Vol.13 (23), p.4193-4196 |
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Hauptverfasser: | , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | Replacement of the morpholine C-ring of linezolid
1 with a 1,3,4-thiadiazolyl ring leads to oxazolidinone analogues
5 having potent antibacterial activity against both gram-positive and gram-negative organisms. Conversion of the C5 acetamide group to a thioacetamide further increases the potency of these compounds.
Replacement of the morpholine C-ring of linezolid
1 with a 1,3,4-thiadiazolyl ring leads to oxazolidinone analogues
5 having potent antibacterial activity against both gram-positive and gram-negative organisms. Conversion of the C5 acetamide group to a thioacetamide further increases the potency of these compounds. |
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ISSN: | 0960-894X 1464-3405 |
DOI: | 10.1016/j.bmcl.2003.07.018 |