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Aerobic Conditions

This means the reaction takes place in the presence of oxygen from the air. Oxygen is used as an oxidant in the reaction.

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Articles of Aerobic Conditions

Cs₂CO₃-Catalyzed Aerobic Oxidative Cross-Dehydrogenative Coupling of Thiols with Phosphonates and Arenes
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- 2-(DIMETHYLAMINO)ETHANETHIOL
Novel bis(oxazole) pincer ligands for catalysis: Application in Suzuki-Miyaura cross coupling reactions under aerobic conditions
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- [PdBr(C₆H₃(C₃NOH(OC₂H₅))2)]
A copper- and solvent-free coupling of acid chlorides with terminal alkynes catalyzed by a polystyrene-supported palladium(0) complex under aerobic conditions
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- C₁₃H₁₃ClO
The design and synthesis of bis(thiourea) ligands and their application in Pd-catalyzed heck and suzuki reactions under aerobic conditions
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A simple and efficient one-pot synthesis of substituted benzo[b]furans by sonogashira coupling-5-endo-dig cyclization catalyzed by palladium nanoparticles in water under ligand- and copper-free aerobic conditions
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- Benzofuran, 5-bromo-2-phenyl-
The enzymatic conversion of exomethylene cephalosporin C into deacetyl cephalosporin C and the role of molecular oxygen in cephalosporin C biosynthesis
Related Chemicals
- (2R,6R,7R)-1-aza-3-methylene-7-<5R-5-p-nitrobenzyloxycarbonylamino-5-p-nitrobenzyloxycarbonylpentaamido>-8-oxo-5-thia-bicyclo<4.2.0>octane-2-carboxylic acid p-nitrobenzyl ester

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Related entries

Oxidation Spectrophotometry Regioselectivity Green chemistry NMR spectroscopy Terminal alkynes Heck reaction Kinetic studies Catalyzed Chromatography Mass spectrometry (MS) one-pot synthesis Reaction pathways Substituted Palladium Nanoparticles Structure Hydroxylation Water as Solvent Substrate Specificity Thiols Phosphonates Arenes Catalytic Efficiency Sonogashira Coupling Fermentation Enzyme Catalysis Synthetic Applications Tuning Properties Overview Biosynthesis In vitro assay 5-Endo-dig cyclization Acid chlorides Pd-Catalyzed Metabolic pathway In vivo study Cofactor Suzuki reaction Benzo[b]furans Enzymatic conversion Ligand-free conditions Reaction intermediate Molecular oxygen (O?)

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