#catalysis — Public Fediverse posts
Live and recent posts from across the Fediverse tagged #catalysis, aggregated by home.social.
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#RobSelects paper of the week #J_A_C_S: Pincer-ligated cobalt-catalyzed four-component carbocarbonylation to form unsymmetric aliphatic ketones. #catalysis https://doi.org/10.1021/jacs.6c06343
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#RobSelects paper of the week #J_A_C_S: Pincer-ligated cobalt-catalyzed four-component carbocarbonylation to form unsymmetric aliphatic ketones. #catalysis https://doi.org/10.1021/jacs.6c06343
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#RobSelects paper of the week #J_A_C_S: Pincer-ligated cobalt-catalyzed four-component carbocarbonylation to form unsymmetric aliphatic ketones. #catalysis https://doi.org/10.1021/jacs.6c06343
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#RobSelects paper of the week #J_A_C_S: Pincer-ligated cobalt-catalyzed four-component carbocarbonylation to form unsymmetric aliphatic ketones. #catalysis https://doi.org/10.1021/jacs.6c06343
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#RobSelects paper of the week #J_A_C_S: Pincer-ligated cobalt-catalyzed four-component carbocarbonylation to form unsymmetric aliphatic ketones. #catalysis https://doi.org/10.1021/jacs.6c06343
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#RobSelects preprint of the week #ChemRxiv: Nickel-catalyzed Suzuki-Miyaura cross coupling of ketones with boronic esters via in-situ ketone derivatization. #catalysis https://doi.org/10.26434/chemrxiv.15003005/v1
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#RobSelects preprint of the week #ChemRxiv: Nickel-catalyzed Suzuki-Miyaura cross coupling of ketones with boronic esters via in-situ ketone derivatization. #catalysis https://doi.org/10.26434/chemrxiv.15003005/v1
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#RobSelects preprint of the week #ChemRxiv: Nickel-catalyzed Suzuki-Miyaura cross coupling of ketones with boronic esters via in-situ ketone derivatization. #catalysis https://doi.org/10.26434/chemrxiv.15003005/v1
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#RobSelects preprint of the week #ChemRxiv: Nickel-catalyzed Suzuki-Miyaura cross coupling of ketones with boronic esters via in-situ ketone derivatization. #catalysis https://doi.org/10.26434/chemrxiv.15003005/v1
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#RobSelects preprint of the week #ChemRxiv: Nickel-catalyzed Suzuki-Miyaura cross coupling of ketones with boronic esters via in-situ ketone derivatization. #catalysis https://doi.org/10.26434/chemrxiv.15003005/v1
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#RobSelects paper of the week #J_A_C_S: Coupling between two tetrahedral carbon centers from an amine and a carboxylic acid catalyzed by an iron porphyrin forming quaternary carbons. #catalysis https://doi.org/10.1021/jacs.6c05065
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#RobSelects paper of the week #J_A_C_S: Coupling between two tetrahedral carbon centers from an amine and a carboxylic acid catalyzed by an iron porphyrin forming quaternary carbons. #catalysis https://doi.org/10.1021/jacs.6c05065
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#RobSelects paper of the week #J_A_C_S: Coupling between two tetrahedral carbon centers from an amine and a carboxylic acid catalyzed by an iron porphyrin forming quaternary carbons. #catalysis https://doi.org/10.1021/jacs.6c05065
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#RobSelects paper of the week #J_A_C_S: Coupling between two tetrahedral carbon centers from an amine and a carboxylic acid catalyzed by an iron porphyrin forming quaternary carbons. #catalysis https://doi.org/10.1021/jacs.6c05065
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#RobSelects preprint of the week #ChemRxiv: Palladium-copper co-catalyzed carbenylative Buchwald-Hartwig coupling between aryl halides, N-tosylhydrazones, and anilines. #catalysis https://doi.org/10.26434/chemrxiv.15002705/v1
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#RobSelects preprint of the week #ChemRxiv: Palladium-copper co-catalyzed carbenylative Buchwald-Hartwig coupling between aryl halides, N-tosylhydrazones, and anilines. #catalysis https://doi.org/10.26434/chemrxiv.15002705/v1
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#RobSelects preprint of the week #ChemRxiv: Palladium-copper co-catalyzed carbenylative Buchwald-Hartwig coupling between aryl halides, N-tosylhydrazones, and anilines. #catalysis https://doi.org/10.26434/chemrxiv.15002705/v1
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#RobSelects preprint of the week #ChemRxiv: Palladium-copper co-catalyzed carbenylative Buchwald-Hartwig coupling between aryl halides, N-tosylhydrazones, and anilines. #catalysis https://doi.org/10.26434/chemrxiv.15002705/v1
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https://www.europesays.com/ie/470324/ Earliest Organisms on Earth Built Their Biochemistry around Molybdenum, Study Suggests #Archaea #Archean #bacteria #Catalysis #Cell #DNA #EarlyEarth #Earth #Éire #Enzyme #Gene #Genome #IE #Ireland #Metabolism #Metal #microbe #Molybdenum #Protein #Science #Tungsten
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#RobSelects preprint of the week #ChemRxiv: Stereoselective nickel metallaphotoredox-catalyzed carbon-carbon cross-coupling of alcohols with gem-dibromoalkenes. #catalysis https://doi.org/10.26434/chemrxiv.15002635/v1
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#RobSelects preprint of the week #ChemRxiv: Stereoselective nickel metallaphotoredox-catalyzed carbon-carbon cross-coupling of alcohols with gem-dibromoalkenes. #catalysis https://doi.org/10.26434/chemrxiv.15002635/v1
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#RobSelects preprint of the week #ChemRxiv: Stereoselective nickel metallaphotoredox-catalyzed carbon-carbon cross-coupling of alcohols with gem-dibromoalkenes. #catalysis https://doi.org/10.26434/chemrxiv.15002635/v1
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#RobSelects preprint of the week #ChemRxiv: Stereoselective nickel metallaphotoredox-catalyzed carbon-carbon cross-coupling of alcohols with gem-dibromoalkenes. #catalysis https://doi.org/10.26434/chemrxiv.15002635/v1
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#RobSelects paper of the week ScienceMagazine: Diastereoselective silver-catalyzed carbon-hydrogen activation and carbon-nitrogen bond formation with chiral sulfonimidamide reactants. #catalysis https://doi.org/10.1126/science.aee3321
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#RobSelects paper of the week ScienceMagazine: Diastereoselective silver-catalyzed carbon-hydrogen activation and carbon-nitrogen bond formation with chiral sulfonimidamide reactants. #catalysis https://doi.org/10.1126/science.aee3321
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#RobSelects paper of the week ScienceMagazine: Diastereoselective silver-catalyzed carbon-hydrogen activation and carbon-nitrogen bond formation with chiral sulfonimidamide reactants. #catalysis https://doi.org/10.1126/science.aee3321
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#RobSelects paper of the week ScienceMagazine: Diastereoselective silver-catalyzed carbon-hydrogen activation and carbon-nitrogen bond formation with chiral sulfonimidamide reactants. #catalysis https://doi.org/10.1126/science.aee3321
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#RobSelects paper of the week #NatureCatalysis: Atroposelective nucleophilic aromatic substitution of fluoronaphthalenes with phenols catalyzed by a chiral phosphonium salt. #catalysis https://doi.org/10.1038/s41929-026-01522-x
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#RobSelects paper of the week #NatureCatalysis: Atroposelective nucleophilic aromatic substitution of fluoronaphthalenes with phenols catalyzed by a chiral phosphonium salt. #catalysis https://doi.org/10.1038/s41929-026-01522-x
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#RobSelects paper of the week #NatureCatalysis: Atroposelective nucleophilic aromatic substitution of fluoronaphthalenes with phenols catalyzed by a chiral phosphonium salt. #catalysis https://doi.org/10.1038/s41929-026-01522-x
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#RobSelects paper of the week #NatureCatalysis: Atroposelective nucleophilic aromatic substitution of fluoronaphthalenes with phenols catalyzed by a chiral phosphonium salt. #catalysis https://doi.org/10.1038/s41929-026-01522-x
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#RobSelects paper of the week #ScienceMagazine: Carbazole-substituted pyridine bis(oxazoline) complexes as a readily accessible family of potent chiral photocatalysts. #catalysis https://doi.org/10.1126/science.aeb5832
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#RobSelects paper of the week #ScienceMagazine: Carbazole-substituted pyridine bis(oxazoline) complexes as a readily accessible family of potent chiral photocatalysts. #catalysis https://doi.org/10.1126/science.aeb5832
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#RobSelects paper of the week #ScienceMagazine: Carbazole-substituted pyridine bis(oxazoline) complexes as a readily accessible family of potent chiral photocatalysts. #catalysis https://doi.org/10.1126/science.aeb5832
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#RobSelects paper of the week #ScienceMagazine: Carbazole-substituted pyridine bis(oxazoline) complexes as a readily accessible family of potent chiral photocatalysts. #catalysis https://doi.org/10.1126/science.aeb5832
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#RobSelects preprint of the week #ChemRxiv: Methylbutyl boronate salt as methylation reagent in Suzuki-Miyaura cross couplings. #catalysis https://doi.org/10.26434/chemrxiv.15001572/v1
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#RobSelects preprint of the week #ChemRxiv: Methylbutyl boronate salt as methylation reagent in Suzuki-Miyaura cross couplings. #catalysis https://doi.org/10.26434/chemrxiv.15001572/v1
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#RobSelects preprint of the week #ChemRxiv: Methylbutyl boronate salt as methylation reagent in Suzuki-Miyaura cross couplings. #catalysis https://doi.org/10.26434/chemrxiv.15001572/v1
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#RobSelects preprint of the week #ChemRxiv: Methylbutyl boronate salt as methylation reagent in Suzuki-Miyaura cross couplings. #catalysis https://doi.org/10.26434/chemrxiv.15001572/v1
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Why can't we just reverse the Haber-Bosch process?
In the latest episode, I talk to Prof. Malte Behrens @SolidStateChemCatal_Kiel about ammonia as a possible hydrogen carrier.
We dive deep into the chemistry of ammonia cracking and explain why the classic iron catalyst loses its activity. Find out how alloying iron with cobalt might just be the solution to unlocking green energy transport via ammonia!
Listen here: https://innovateandreact.com/why-reversing-the-haber-bosch-process-requires-a-new-catalyst/
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#RobSelects paper of the week #J_A_C_S: Asymmetric Sm-catalyzed carbon-carbon coupling between alkenes and ketones forming tertiary alcohols. #catalysis https://doi.org/10.1021/jacs.5c20884
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Interesting talk by Danny Broere of the University of Utrecht at #Lunteren2026. He gave exciting insights into equipping metal complexes with new functions by exploiting metal-ligand cooperativity.
https://pubs.acs.org/doi/abs/10.1021/jacs.5c15308
#Chemistry #Catalysis #MetalComplexes -
Interesting talk by Danny Broere of the University of Utrecht at #Lunteren2026. He gave exciting insights into equipping metal complexes with new functions by exploiting metal-ligand cooperativity.
https://pubs.acs.org/doi/abs/10.1021/jacs.5c15308
#Chemistry #Catalysis #MetalComplexes -
Interesting talk by Danny Broere of the University of Utrecht at #Lunteren2026. He gave exciting insights into equipping metal complexes with new functions by exploiting metal-ligand cooperativity.
https://pubs.acs.org/doi/abs/10.1021/jacs.5c15308
#Chemistry #Catalysis #MetalComplexes -
Interesting talk by Danny Broere of the University of Utrecht at #Lunteren2026. He gave exciting insights into equipping metal complexes with new functions by exploiting metal-ligand cooperativity.
https://pubs.acs.org/doi/abs/10.1021/jacs.5c15308
#Chemistry #Catalysis #MetalComplexes -
Interesting talk by Danny Broere of the University of Utrecht at #Lunteren2026. He gave exciting insights into equipping metal complexes with new functions by exploiting metal-ligand cooperativity.
https://pubs.acs.org/doi/abs/10.1021/jacs.5c15308
#Chemistry #Catalysis #MetalComplexes -
As an organic chemist, should you specialize in synthesis method development or total synthesis?
In his inspiring talk at #Lunteren2026, Alois Fürstner from the Max-Planck-Institut für Kohlenforschung shows how his group is excelling at both and makes the point that there is important cross-fertilization between the two research directions in his group.
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As an organic chemist, should you specialize in synthesis method development or total synthesis?
In his inspiring talk at #Lunteren2026, Alois Fürstner from the Max-Planck-Institut für Kohlenforschung shows how his group is excelling at both and makes the point that there is important cross-fertilization between the two research directions in his group.
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As an organic chemist, should you specialize in synthesis method development or total synthesis?
In his inspiring talk at #Lunteren2026, Alois Fürstner from the Max-Planck-Institut für Kohlenforschung shows how his group is excelling at both and makes the point that there is important cross-fertilization between the two research directions in his group.
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As an organic chemist, should you specialize in synthesis method development or total synthesis?
In his inspiring talk at #Lunteren2026, Alois Fürstner from the Max-Planck-Institut für Kohlenforschung shows how his group is excelling at both and makes the point that there is important cross-fertilization between the two research directions in his group.