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  1. Attività

Enabling TECHNOlogies-driven chemistry: a tailored TRAINing research program for batch and flow synthesis of chiral amino derivatives (TECHNOTRAIN)

Progetto
The main aim of “TECHNOTRAIN” proposal (Enabling TECHNOlogies-driven chemistry: a tailored TRAINing research program for batch and flow synthesis of chiral amino derivatives) is to create a training platform for young European researchers, based on the creativity, flexibility and accuracy characteristic of an academic working environment, but with an industrial focus. “TECHNOTRAIN” has the specific objective to develop general, reproducible and also profitable, stereoselective, catalytic synthetic methods applicable for industrial production of enantiomerically pure, functionalized amino derivatives featuring a quaternary stereocenter. Target molecules will be chiral pharmaceutically active ingredients, or immediate precursors, including nonproteogenic alfa-disubstituted-amino acids. The aim is both to synthesize specific target molecules and to develop highly efficient, technology-driven methodologies. Continuous flow processes will be considered, to perform a fast screening of the reaction conditions, and then, with the optimized conditions in hand, to scale up the reaction (by scaling-out or numbering up or scalingup). The combination of two modern, catalytic strategies (photocatalysis and organocatalysis) with safe and environmental friendly technologies (including the use of 3D-printed devices) is a key step towards the development of a more efficient and sustainable chemistry, in line with the Europe strategy. A future generation of scientists will be trained to face the challenges imposed by the transfer the new, green technologies into industrial processes. Another primary objective of “TECHNOTRAIN” is to develop a modern training model for young European researchers, where education is realized through research and a strong interaction between public and private sector. The project wishes to be truly a prototype of an efficient European research training structure aimed at growing young researchers capable of interacting with the private sector research.
  • Dati Generali
  • Pubblicazioni

Dati Generali

Partecipanti

BENAGLIA MAURIZIO   Responsabile scientifico  

Dipartimenti coinvolti

Dipartimento di Chimica   Principale  

Tipo

H20MCITNIF - Horizon 2020_Marie Skłodowska-Curie actions-Innovative Training Network (ITN)/Individual Fellowships (IF)

Finanziatore

EUROPEAN COMMISSION
Organizzazione Esterna Ente Finanziatore

Capofila

UNIVERSITA' DEGLI STUDI DI MILANO

Periodo di attività

Novembre 1, 2018 - Ottobre 31, 2022

Durata progetto

48 mesi

Pubblicazioni

Pubblicazioni (11)

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  • Articolo
Enantioselective Organocatalytic Addition of Nitromethane to Trifluoromethylaryl Ketoimines Promoted by Electron-Rich Bifunctional Iminophosphoranes 
ADVANCED SYNTHESIS & CATALYSIS
WILEY-VCH VERLAG GMBHV
2023
Articolo
Open Access
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Laboratory Scale Continuous Flow Systems for the Enantioselective Phase Transfer Catalytic Synthesis of Quaternary Amino Acids 
MOLECULES
MDPI
2023
Articolo
Open Access
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Stereoselective [2 + 2] photodimerization: a viable strategy for the synthesis of enantiopure cyclobutane derivatives 
ORGANIC & BIOMOLECULAR CHEMISTRY
ROYAL SOCIETY OF CHEMISTRY
2023
Articolo
Open Access
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Synthesis of tetrasubstituted nitroalkenes and preliminary studies of their enantioselective organocatalytic reduction. 
MOLECULES
MDPI
2023
Articolo
Open Access
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Supported Eosin Y as a Photocatalyst for C-H Arylation of Furan in Batch and Flow 
MOLECULES
MDPI
2022
Articolo
Open Access
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Continuous Flow Synthesis of α-Trifluoromethylthiolated Esters and Amides from Carboxylic Acids: A Telescoped Approach 
JOURNAL OF ORGANIC CHEMISTRY
AMERICAN CHEMICAL SOCIETY
2021
Articolo
Open Access
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Nitroalkene reduction in deep eutectic solvents promoted by BH3NH3 
BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY
BEILSTEIN INSTITUT
2021
Articolo
Open Access
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Ammonia-Borane-Mediated Reduction of Nitroalkenes 
SYNOPEN
THIEME
2020
Articolo
Open Access
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Eosin Y : homogeneous photocatalytic in-flow reactions and solid supported-catalysts for in-batch synthetic transformation 
APPLIED SCIENCES
MDPI
2020
Articolo
Open Access
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Quasiperiodic Crystals: Teaching Aperiodicity of a Crystal Lattice with 3D-Printed Penrose Tiles 
JOURNAL OF CHEMICAL EDUCATION
AMERICAN CHEMICAL SOCIETY
2020
Articolo
Reserved Access
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Organocatalytic Michael addition to (D)-mannitol-derived enantiopure nitroalkenes: A valuable strategy for the synthesis of densely functionalized chiral molecules 
MOLECULES
MDPI
2019
Articolo
Open Access
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