ISOF promote excellence in SYNTHETIC CHEMISTRYand PHOTOCHEMISTRY for the design and development of tailored molecules and FUNCTIONAL MATERIALS
News
14 maggio 2026 - COUPON ESAURITI
When we think about...
Events
- Molecular Catalysts Anchored on Metal Oxides for Artificial Photosynthesis
- 4/20/2026-12:0
- 4/29/2026-0:0
- University of Ottawa, Canada
- https://www.isof.cnr.it/wp-content/uploads/2024/06/Fiera-rimini-1024x634-1.png
- Catalytic methods continue to reshape how chemists access fundamental bond constructions in organic synthesis. While many classical transformations rely on preactivated reagents or stoichiometric strategies, our work focuses on achieving familiar reactivity directly from native functional groups such as esters, aldehydes, ketones, and alcohols. By rethinking how these abundant groups can participate in transition metal-catalyzed reactions, we aim to enable traditional synthetic disconnections through more efficient and versatile catalytic pathways. A central challenge in this area is that these systems often exhibit broad or competing reactivity,
- If you would like to follow this PhD thesis defense online, please, register here!
- https://www.isof.cnr.it/2026/04/12/modern-catalysis-for-classical-reactivity-2/
- 0
- Modern Catalysis for Classical Reactivity
- 05/26/2026-12:0
- 5/31/2026-0:0
- University of Ottawa, Canada
- https://www.isof.cnr.it/wp-content/uploads/2024/06/banner-notte-ricercatori-colore2025.png
- Catalytic methods continue to reshape how chemists access fundamental bond constructions in organic synthesis. While many classical transformations rely on preactivated reagents or stoichiometric strategies, our work focuses on achieving familiar reactivity directly from native functional groups such as esters, aldehydes, ketones, and alcohols. By rethinking how these abundant groups can participate in transition metal-catalyzed reactions, we aim to enable traditional synthetic disconnections through more efficient and versatile catalytic pathways. A central challenge in this area is that these systems often exhibit broad or competing reactivity,
- https://www.isof.cnr.it/2026/04/12/modern-catalysis-for-classical-reactivity/
- 0
- Modern Catalysis for Classical Reactivity
- 05/26/2026-12:0
- 5/31/2026-0:0
- University of Ottawa, Canada
- https://www.isof.cnr.it/wp-content/uploads/2024/06/banner-notte-ricercatori-colore2025.png
- Catalytic methods continue to reshape how chemists access fundamental bond constructions in organic synthesis. While many classical transformations rely on preactivated reagents or stoichiometric strategies, our work focuses on achieving familiar reactivity directly from native functional groups such as esters, aldehydes, ketones, and alcohols. By rethinking how these abundant groups can participate in transition metal-catalyzed reactions, we aim to enable traditional synthetic disconnections through more efficient and versatile catalytic pathways. A central challenge in this area is that these systems often exhibit broad or competing reactivity,
- https://www.isof.cnr.it/2026/05/22/modern-catalysis-for-classical-reactivity-3/
- 0