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A Convenient Synthesis of Linezolid Through Buchwald-Hartwig Amination

https://doi.org/10.2139/ssrn.4150601
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/adsc.200800032openalex-extracted
Palladium‐Catalyzed Stille Cross‐Coupling Reaction of Aryl Chlorides using a Pre‐Milled Palladium Acetate and XPhos Catalyst System
inferredcites →https://doi.org/10.1002/anie.200200528openalex-extracted
Oxazolidinone Structure–Activity Relationships Leading to Linezolid
inferredcites →https://doi.org/10.1016/j.bmcl.2003.07.021openalex-extracted
Novel oxazolidinone–quinolone hybrid antimicrobials
inferredcites →https://doi.org/10.1016/j.ejmech.2010.10.015openalex-extracted
Discovery of a novel nitroimidazolyl–oxazolidinone hybrid with potent anti Gram-positive activity: Synthesis and antibacterial evaluation
inferredcites →https://doi.org/10.1021/ol026902hopenalex-extracted
Highly Efficient CuI-Catalyzed Coupling of Aryl Bromides with Oxazolidinones Using Buchwald's Protocol: A Short Route to Linezolid and Toloxatone
inferredcites →https://doi.org/10.1093/jac/33.2.350openalex-extracted
J Antimicrob Chemother 1994; 33: 350–351
inferredcites →https://doi.org/10.2174/138955707780363783openalex-extracted
The Contribution of Oxazolidinone Frame to The Biological Activity of Pharmaceutical Drugs and Natural Products
inferredcites →https://doi.org/10.2174/1568005014606099openalex-extracted
The Discovery of Linezolid, the First Oxazolidinone Antibacterial Agent

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inferred← citeshttps://doi.org/10.2139/ssrn.5392185openalex-snapshot
Comprehensive Electrochemical Study of Linezolid a Synthetic Oxazolidinone Antimicrobial Drug and its Toxicity Mechanism. Electrosynthesis of New Linezolid Derivatives
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