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#catalysis — Public Fediverse posts

Live and recent posts from across the Fediverse tagged #catalysis, aggregated by home.social.

  1. #RobSelects paper of the week #J_A_C_S: Pincer-ligated cobalt-catalyzed four-component carbocarbonylation to form unsymmetric aliphatic ketones. #catalysis doi.org/10.1021/jacs.6c06343

  2. #RobSelects paper of the week #J_A_C_S: Pincer-ligated cobalt-catalyzed four-component carbocarbonylation to form unsymmetric aliphatic ketones. #catalysis doi.org/10.1021/jacs.6c06343

  3. #RobSelects paper of the week #J_A_C_S: Pincer-ligated cobalt-catalyzed four-component carbocarbonylation to form unsymmetric aliphatic ketones. #catalysis doi.org/10.1021/jacs.6c06343

  4. #RobSelects paper of the week #J_A_C_S: Pincer-ligated cobalt-catalyzed four-component carbocarbonylation to form unsymmetric aliphatic ketones. #catalysis doi.org/10.1021/jacs.6c06343

  5. #RobSelects paper of the week #J_A_C_S: Pincer-ligated cobalt-catalyzed four-component carbocarbonylation to form unsymmetric aliphatic ketones. #catalysis doi.org/10.1021/jacs.6c06343

  6. #RobSelects preprint of the week #ChemRxiv: Nickel-catalyzed Suzuki-Miyaura cross coupling of ketones with boronic esters via in-situ ketone derivatization. #catalysis doi.org/10.26434/chemrxiv.1500

  7. #RobSelects preprint of the week #ChemRxiv: Nickel-catalyzed Suzuki-Miyaura cross coupling of ketones with boronic esters via in-situ ketone derivatization. #catalysis doi.org/10.26434/chemrxiv.1500

  8. #RobSelects preprint of the week #ChemRxiv: Nickel-catalyzed Suzuki-Miyaura cross coupling of ketones with boronic esters via in-situ ketone derivatization. #catalysis doi.org/10.26434/chemrxiv.1500

  9. #RobSelects preprint of the week #ChemRxiv: Nickel-catalyzed Suzuki-Miyaura cross coupling of ketones with boronic esters via in-situ ketone derivatization. #catalysis doi.org/10.26434/chemrxiv.1500

  10. #RobSelects preprint of the week #ChemRxiv: Nickel-catalyzed Suzuki-Miyaura cross coupling of ketones with boronic esters via in-situ ketone derivatization. #catalysis doi.org/10.26434/chemrxiv.1500

  11. #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 doi.org/10.1021/jacs.6c05065

  12. #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 doi.org/10.1021/jacs.6c05065

  13. #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 doi.org/10.1021/jacs.6c05065

  14. #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 doi.org/10.1021/jacs.6c05065

  15. #RobSelects preprint of the week #ChemRxiv: Palladium-copper co-catalyzed carbenylative Buchwald-Hartwig coupling between aryl halides, N-tosylhydrazones, and anilines. #catalysis doi.org/10.26434/chemrxiv.1500

  16. #RobSelects preprint of the week #ChemRxiv: Palladium-copper co-catalyzed carbenylative Buchwald-Hartwig coupling between aryl halides, N-tosylhydrazones, and anilines. #catalysis doi.org/10.26434/chemrxiv.1500

  17. #RobSelects preprint of the week #ChemRxiv: Palladium-copper co-catalyzed carbenylative Buchwald-Hartwig coupling between aryl halides, N-tosylhydrazones, and anilines. #catalysis doi.org/10.26434/chemrxiv.1500

  18. #RobSelects preprint of the week #ChemRxiv: Palladium-copper co-catalyzed carbenylative Buchwald-Hartwig coupling between aryl halides, N-tosylhydrazones, and anilines. #catalysis doi.org/10.26434/chemrxiv.1500

  19. #RobSelects preprint of the week #ChemRxiv: Stereoselective nickel metallaphotoredox-catalyzed carbon-carbon cross-coupling of alcohols with gem-dibromoalkenes. #catalysis doi.org/10.26434/chemrxiv.1500

  20. #RobSelects preprint of the week #ChemRxiv: Stereoselective nickel metallaphotoredox-catalyzed carbon-carbon cross-coupling of alcohols with gem-dibromoalkenes. #catalysis doi.org/10.26434/chemrxiv.1500

  21. #RobSelects preprint of the week #ChemRxiv: Stereoselective nickel metallaphotoredox-catalyzed carbon-carbon cross-coupling of alcohols with gem-dibromoalkenes. #catalysis doi.org/10.26434/chemrxiv.1500

  22. #RobSelects preprint of the week #ChemRxiv: Stereoselective nickel metallaphotoredox-catalyzed carbon-carbon cross-coupling of alcohols with gem-dibromoalkenes. #catalysis doi.org/10.26434/chemrxiv.1500

  23. #RobSelects paper of the week ScienceMagazine: Diastereoselective silver-catalyzed carbon-hydrogen activation and carbon-nitrogen bond formation with chiral sulfonimidamide reactants. #catalysis doi.org/10.1126/science.aee3321

  24. #RobSelects paper of the week ScienceMagazine: Diastereoselective silver-catalyzed carbon-hydrogen activation and carbon-nitrogen bond formation with chiral sulfonimidamide reactants. #catalysis doi.org/10.1126/science.aee3321

  25. #RobSelects paper of the week ScienceMagazine: Diastereoselective silver-catalyzed carbon-hydrogen activation and carbon-nitrogen bond formation with chiral sulfonimidamide reactants. #catalysis doi.org/10.1126/science.aee3321

  26. #RobSelects paper of the week ScienceMagazine: Diastereoselective silver-catalyzed carbon-hydrogen activation and carbon-nitrogen bond formation with chiral sulfonimidamide reactants. #catalysis doi.org/10.1126/science.aee3321

  27. #RobSelects paper of the week #NatureCatalysis: Atroposelective nucleophilic aromatic substitution of fluoronaphthalenes with phenols catalyzed by a chiral phosphonium salt. #catalysis doi.org/10.1038/s41929-026-015

  28. #RobSelects paper of the week #NatureCatalysis: Atroposelective nucleophilic aromatic substitution of fluoronaphthalenes with phenols catalyzed by a chiral phosphonium salt. #catalysis doi.org/10.1038/s41929-026-015

  29. #RobSelects paper of the week #NatureCatalysis: Atroposelective nucleophilic aromatic substitution of fluoronaphthalenes with phenols catalyzed by a chiral phosphonium salt. #catalysis doi.org/10.1038/s41929-026-015

  30. #RobSelects paper of the week #NatureCatalysis: Atroposelective nucleophilic aromatic substitution of fluoronaphthalenes with phenols catalyzed by a chiral phosphonium salt. #catalysis doi.org/10.1038/s41929-026-015

  31. #RobSelects paper of the week #ScienceMagazine: Carbazole-substituted pyridine bis(oxazoline) complexes as a readily accessible family of potent chiral photocatalysts. #catalysis doi.org/10.1126/science.aeb5832

  32. #RobSelects paper of the week #ScienceMagazine: Carbazole-substituted pyridine bis(oxazoline) complexes as a readily accessible family of potent chiral photocatalysts. #catalysis doi.org/10.1126/science.aeb5832

  33. #RobSelects paper of the week #ScienceMagazine: Carbazole-substituted pyridine bis(oxazoline) complexes as a readily accessible family of potent chiral photocatalysts. #catalysis doi.org/10.1126/science.aeb5832

  34. #RobSelects paper of the week #ScienceMagazine: Carbazole-substituted pyridine bis(oxazoline) complexes as a readily accessible family of potent chiral photocatalysts. #catalysis doi.org/10.1126/science.aeb5832

  35. #RobSelects preprint of the week #ChemRxiv: Methylbutyl boronate salt as methylation reagent in Suzuki-Miyaura cross couplings. #catalysis doi.org/10.26434/chemrxiv.1500

  36. #RobSelects preprint of the week #ChemRxiv: Methylbutyl boronate salt as methylation reagent in Suzuki-Miyaura cross couplings. #catalysis doi.org/10.26434/chemrxiv.1500

  37. #RobSelects preprint of the week #ChemRxiv: Methylbutyl boronate salt as methylation reagent in Suzuki-Miyaura cross couplings. #catalysis doi.org/10.26434/chemrxiv.1500

  38. #RobSelects preprint of the week #ChemRxiv: Methylbutyl boronate salt as methylation reagent in Suzuki-Miyaura cross couplings. #catalysis doi.org/10.26434/chemrxiv.1500

  39. 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: innovateandreact.com/why-rever

    #Chemistry #Catalysis #Ammonia

  40. #RobSelects paper of the week #J_A_C_S: Asymmetric Sm-catalyzed carbon-carbon coupling between alkenes and ketones forming tertiary alcohols. #catalysis doi.org/10.1021/jacs.5c20884

  41. 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.

    pubs.acs.org/doi/abs/10.1021/j
    #Chemistry #Catalysis #MetalComplexes

  42. 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.

    pubs.acs.org/doi/abs/10.1021/j
    #Chemistry #Catalysis #MetalComplexes

  43. 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.

    pubs.acs.org/doi/abs/10.1021/j
    #Chemistry #Catalysis #MetalComplexes

  44. 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.

    pubs.acs.org/doi/abs/10.1021/j
    #Chemistry #Catalysis #MetalComplexes

  45. 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.

    pubs.acs.org/doi/abs/10.1021/j
    #Chemistry #Catalysis #MetalComplexes

  46. 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.

    #Chemistry #Synthesis #Catalysis

  47. 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.

    #Chemistry #Synthesis #Catalysis

  48. 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.

    #Chemistry #Synthesis #Catalysis

  49. 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.

    #Chemistry #Synthesis #Catalysis