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Experimental and theoretical investigations on the cephalosporin Δ3Δ2 isomerization

https://doi.org/10.1002/ejtc.10
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inferred← citeshttps://doi.org/10.2139/ssrn.4606423openalex-extracted
Identification, Synthesis, Isolation, and Characterization of Formulation Related Degradation Impurity of Cefadroxil Oral Suspension
inferred← citeshttps://doi.org/10.1016/j.jchromb.2025.124537openalex-snapshot
Identification, synthesis, isolation, and characterization of formulation related degradation impurity of Cefadroxil Oral suspension
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)00445-8openalex-snapshot
Chair–boat equilibrium as driving force in epimerization of 3,7-dimethylbicyclo[3.3.1]nonan-2,9-dione derivatives. Stereocontrolled synthesis of the 3- exo ,7 -exo - and 3- endo ,7- exo -dimethylbicyclo[3.3.1]nonan-9-ones
inferred← citeshttps://doi.org/10.1016/s0040-4039(97)00588-1openalex-snapshot
Palladium-catalysed reduction of 3-substituted cephems. A high yield approach to ceftizoxime synthetic intermediates
inferred← citeshttps://doi.org/10.1039/c0md00015aopenalex-snapshot
Syntheses and biological evaluation of new cephalosporin-oxazolidinone conjugates
inferred← citeshttps://doi.org/10.1039/d5nj00243eopenalex-snapshot
Functionalization at the C3 position of the cephalosporin pharmacophore by palladium-catalyzed cross-coupling reactions
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