Molecules | Free Full-Text | New Estrone Oxime Derivatives: Synthesis, Cytotoxic Evaluation and Docking Studies
Synthesis and Biological Evaluation of d-Amino Acid Oxidase Inhibitors | Journal of Medicinal Chemistry
Oxime A and nitroso B tautomeric forms of AQM. | Download Scientific Diagram
Efficient γ-amino-proline-derived cell penetrating peptide–superparamagnetic iron oxide nanoparticle conjugates via aniline-catalyzed oxime chemistry as bimodal imaging nanoagents - Chemical Communications (RSC Publishing)
SPECT findings in patients with primary mania
Typical GC–NICI-MS chromatograms of O-PFB-oxime- TMS derivatives of HNE... | Download Scientific Diagram
PDF) A newly developed oxime K203 is the most effective reactivator of tabun-inhibited acetylcholinesterase
Non-quaternary oximes detoxify nerve agents and reactivate nerve agent-inhibited human butyrylcholinesterase | Communications Biology
Enantioselective Synthesis of Chiral Oxime Ethers: Desymmetrization and Dynamic Kinetic Resolution of Substituted Cyclohexanones,Angewandte Chemie International Edition - X-MOL
Dissociation or Cyclization: Options for a Triad of Radicals Released from Oxime Carbamates | Journal of the American Chemical Society
Asymmetric Hydrogenation of Oximes Synergistically Assisted by Lewis and Brønsted Acids | Journal of the American Chemical Society
Chemical Reactivity Measurement and the Predictive Identification of Skin Sensitisers: The Report and Recommendations of ECVAM Workshop 64a - Frank Gerberick, Maja Aleksic, David Basketter, Silvia Casati, Ann-Therese Karlberg, Petra Kern, Ian
The role of Cinnamomum zeylanicum essential oil, (E)‐cinnamaldehyde and (E)‐cinnamaldehyde oxime in the control of Meloidogyne incognita - Ferreira Barros - 2021 - Journal of Phytopathology - Wiley Online Library
![O-[2-Hydroxy-3-(dialkylamino)propyl]ethers of (+)-1,7,7-trimethyl bicyclo[2.2.1]heptan-2-one oxime (camphor oxime) with analgesic and antiarrhythmic activities - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0014827X00000653-sc1.gif "O-[2-Hydroxy-3-(dialkylamino)propyl]ethers of (+)-1,7,7-trimethyl bicyclo[2.2.1]heptan-2-one oxime (camphor oxime) with analgesic and antiarrhythmic activities - ScienceDirect")
O-[2-Hydroxy-3-(dialkylamino)propyl]ethers of (+)-1,7,7-trimethyl bicyclo[2.2.1]heptan-2-one oxime (camphor oxime) with analgesic and antiarrhythmic activities - ScienceDirect
Confirmations of oximes by coinjection of headspace sample collected... | Download Scientific Diagram
Oxime Amides as a Novel Zinc Binding Group in Histone Deacetylase Inhibitors: Synthesis, Biological Activity, and Computational Evaluation | Journal of Medicinal Chemistry
Fluorinated Heterocyclic Compounds. An Effective Strategy for the Synthesis of Fluorinated Z-Oximes of 3-Perfluoroalkyl-6-phenyl-2H-1,2,4-triazin- 5-ones via a Ring-Enlargement Reaction of 3-Benzoyl-5-perfluoroalkyl-1,2,4-oxadiazoles and Hydrazine ...
Nanoparticulate Transport of Oximes over an In Vitro Blood-Brain Barrier Model | PLOS ONE
Fast‐relaxing dynamic hydrogel further reduced the undesired... | Download Scientific Diagram
PDF) Effects of Acetone O-(2-naphtylsulphonyl)oxime Pre-application on Maize Seedlings Under Cadmium Stress
Non-quaternary oximes detoxify nerve agents and reactivate nerve agent-inhibited human butyrylcholinesterase | Communications Biology
Docking studies and effects of syn-anti isomery of oximes derived from pyridine imidazol bicycled systems as potential human acetylcholinesterase reactivators - ScienceDirect
![Copper-Catalyzed Tandem [2,3]-Rearrangement and 6π-3-Azatriene Electrocyclization in (E)-O-Propargylic α,β-Unsaturated Oximes | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/ja102436z/asset/images/large/ja-2010-02436z_0004.jpeg "Copper-Catalyzed Tandem [2,3]-Rearrangement and 6π-3-Azatriene Electrocyclization in (E)-O-Propargylic α,β-Unsaturated Oximes | Journal of the American Chemical Society")
Copper-Catalyzed Tandem [2,3]-Rearrangement and 6π-3-Azatriene Electrocyclization in (E)-O-Propargylic α,β-Unsaturated Oximes | Journal of the American Chemical Society
