Development of novel strategies for alkyl organoboron preparation via boryl radical reactivity

Informazioni relative al progetto

BRADOCO

ID dell’accordo di sovvenzione: 101150093

DOI

10.3030/101150093

Progetto chiuso

Data della firma CE 4 Aprile 2024

Data di avvio 3 Giugno 2024

Data di completamento 2 Giugno 2026

Finanziato da

• Marie Skłodowska-Curie Actions (MSCA)

Costo totale

Nessun dato

Contributo UE

€ 173 847,36

Coordinato da

RHEINISCH-WESTFAELISCHE TECHNISCHE HOCHSCHULE AACHEN
Germany

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I link ai risultati e alle pubblicazioni dei progetti del 7° PQ, così come i link ad alcuni tipi di risultati specifici come dataset e software, sono recuperati dinamicamente da .OpenAIRE .

Risultati finali

Documents, reports (1)

Communication, Dissemination & Exploitation Plan

The plan describes the planned measures to maximize the impact ofthe project, including the dissemination and exploitation measures that are planned, and the target group(s) addressed. Regarding communication measuresand public engagement strategy, the aim is to inform and reach out to society andshow the activities performed, and the use and the benefits the project will have forcitizens.

Data Management Plan (1)

Data Management Plan

The Data Management Plan describes the data management life cyclefor all data sets that will be collected, processed or generated by the action. It is adocument describing what data will be collected, processed or generated andfollowing what methodology and standards, whether and how this data will beshared and/or made open, and how it will be curated and preserved.

Pubblicazioni

Peer reviewed articles (5)

Asymmetric hydrogenation of 3 <i>H</i> -azepines <i>via</i> catalytic kinetic resolution: access to <i>anti</i> -disubstituted azepanes

Autori: Linda Bui, Dilara Berna Yildiz, Diego García Matesanz, Esteban Matador, Raquel Sanchez, Iuliana Atodiresei, Giovanni Lonardi, Daniele Leonori
Pubblicato in: Chemical Science, Numero 17, 2026, ISSN 2041-6520
Editore: Royal Society of Chemistry (RSC)
DOI: 10.1039/D6SC01819J

Deaminative cross-coupling of amines by boryl radical β-scission

Autori: Zhenhua Zhang, Giovanni Lonardi, Thomas Sephton, Yusuf C. Guersoy, Chiara Stavagna, Giovanni V. A. Lenardon, Massimo Bietti, Daniele Leonori
Pubblicato in: Nature, Numero 647, 2025, ISSN 0028-0836
Editore: Springer Science and Business Media LLC
DOI: 10.1038/S41586-025-09725-1

Excited‐State Basicity Diverts the Site‐Selectivity of Aromatic Deuteration: Application to the Late‐Stage Labeling of Pharmaceuticals

Autori: Eva Rivera‐Chao, Javier Corpas, Giovanni Lonardi, Volker Derdau, Alessandro Ruffoni, Daniele Leonori
Pubblicato in: Angewandte Chemie International Edition, Numero 64, 2025, ISSN 1433-7851
Editore: Wiley
DOI: 10.1002/ANIE.202500627

Importance of Polar Effects in Halogen-Atom Transfer from Alkyl Iodides to α-Aminoalkyl Radicals. A Kinetic and Computational Evaluation of the Role of Structural and Medium Effects

Autori: Jacopo Mancini, Chiara Stavagna, Francesco Pileri, Giovanni Lonardi, Enrique M. Arpa, Marco Galeotti, Sergio Sisti, Fabio Juliá, Michela Salamone, Daniele Leonori, Massimo Bietti
Pubblicato in: JACS Au, Numero 6, 2026, ISSN 2691-3704
Editore: American Chemical Society (ACS)
DOI: 10.1021/JACSAU.5C00920

Photochemical permutation of meta-substituted phenols

Autori: Maialen Alonso, Giovanni Lonardi, Enrique M. Arpa, Baptiste Roure, Alessandro Ruffoni, Daniele Leonori
Pubblicato in: Nature Communications, Numero 16, 2025, ISSN 2041-1723
Editore: Springer Science and Business Media LLC
DOI: 10.1038/S41467-025-62549-5