Andrea Palone
University of Bologna, Universitat de Girona, University of Rome Tor Vergata
Research areas: Chemistry · Inorganic Chemistry · Crystal structures of chemical compounds · Crystallography and molecular interactions · Crystal Structures and Properties
About
Dr. Andrea Palone is a chemist specializing in hydrogen atom transfer (HAT) strategies in catalysis. He earned his Ph.D. in Chemistry from the Universitat de Girona in collaboration with the Università di Roma "Tor Vergata," under the supervision of Prof. Miquel Costas and Prof. Massimo Bietti.
His work was recognized in 2024 with the Lilly Prize in collaboration with RSEQ.
Currently, he is a postdoctoral researcher in the Melchiorre group at the Università di Bologna.
Employment
- 2024 - Present
- 2019 - 2024
Education
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University of Rome Tor Vergata Master Cum Laude2016 - 2018
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University of Rome Tor Vergata Bachelor2012 - 2016
Projects & Funding
Projects & funding information is unavailable.
Publications (12)
- Electron Donor–Acceptor Complex Catalysis in Synthetic Chemistry Save
- Stereoretentive Norrish–Yang Photocyclization Mediated by Hydrogen Bonding Save
- Light-Driven Organocatalytic Birch Reduction for Late-Stage Drug Modification and sp3-Rich Spirocycle Synthesis Save
- Shaping of a Reactive Manganese Catalyst Enables Access to Polyfunctionalized Cyclohexanes via Enantioselective C(sp3)─H Bond Oxidation of 1,3‐meso Diethers Save
- Enzymatic and Bio-Inspired Enantioselective Oxidation of Non-Activated C(sp 3)–H Bonds Save
- Understanding Catalytic Enantioselective C–H Bond Oxidation at Nonactivated Methylenes Through Predictive Statistical Modeling Analysis Save
- Strain Release in Hydrogen Atom Transfer from 1,4-Disubstituted Cyclohexanes to the Cumyloxy Radical Save
- tert‐Butyl as a Functional Group: Non‐Directed Catalytic Hydroxylation of Sterically Congested Primary C−H Bonds Save
- Highly Enantioselective Catalytic Lactonization at Nonactivated Primary and Secondary γ-C–H Bonds Save
- C–H Bonds as Functional Groups: Simultaneous Generation of Multiple Stereocenters by Enantioselective Hydroxylation at Unactivated Tertiary C–H Bonds Save
- 2.12 Asymmetric C—H Oxidation with Biologically Inspired Manganese and Iron Catalysts Save
- Carboxylic Acid Directed γ-Lactonization of Unactivated Primary C–H Bonds Catalyzed by Mn Complexes: Application to Stereoselective Natural Product Diversification Save