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

Informacje na temat projektu

TECHNOTRAIN

Identyfikator umowy o grant: 812944

DOI 10.3030/812944

Projekt został zamknięty

Data podpisania przez KE 19 Lipca 2018

Data rozpoczęcia 1 Listopada 2018

Data zakończenia 31 Października 2022

Finansowanie w ramach

• EXCELLENT SCIENCE - Marie Skłodowska-Curie Actions

Koszt całkowity € 784 499,04

Wkład UE € 784 499,04

Koordynowany przez

UNIVERSITA DEGLI STUDI DI MILANO
Italy

Rezultaty

Other (6)

recruitment

Selection process completed

seminar microreactor

1 Day seminar on microreactors completed

ESR positions

ESR positions advertised

Oureach events

Participation of the ESRs to one, or more, of the outreach events listed in Section 2.3

enrolment

Enrolment of the ESRs to the Doctorate School UMIL

Workshop on LCA and Carbon Footprint Eval. done

Workshop on LCA and Carbon Footprint Evaluation done

Documents, reports (8)

PhD report 1

Annual reports presented at PhD School of UMIL

brochure

Preparation of brochures presenting the TECHNOTRAIN consortium

PhD Theses

PhD theses written by the ESRs

Supervisory Board

Supervisory Board of the network established

PhD report 3

Annual reports presented at PhD School of UMIL

PhD report 2

Annual reports presented at PhD School of UMIL

publications

At least 15 Scientific publications on international journals

Publication of articles in the non- specialised press

Publication of articles in the non specialised press

Websites, patent fillings, videos etc. (1)

web site

Project web site up and running

Publikacje

Peer reviewed articles (7)

Nitroalkene reduction in deep eutectic solvents promoted by BH3NH3.

Autorzy: Chiara Faverio; Monica Fiorenza Boselli; Patricia Camarero Gonzalez; Alessandra Puglisi; Maurizio Benaglia
Opublikowane w: Beilstein Journal of Organic Chemistry, Vol 17, Iss 1, Pp 1041-1047 (2021), Numer 2, 2021, Strona(/y) 1041–1047, ISSN 1860-5397
Wydawca: Beilstein-Institut
DOI: 10.3762/bjoc.17.83

In flow enantioselective homogeneous organic synthesis

Autorzy: A. Puglisi, S. Rossi, F. Herbrik, F. Medici, M. Benaglia
Opublikowane w: Green Processing and Synthesis, 2021, Strona(/y) 1-11, ISSN 2191-9542
Wydawca: Walter de Gruyter and Co.
DOI: 10.1515/gps-2021-0073

Enantioselective organophotocatalytic telescoped synthesis of a chiral privileged active pharmaceutical ingredient

Autorzy: F. Herbrik , M. Sanz, A. Puglisi, S. Rossi, M. Benaglia
Opublikowane w: Chemistry a European Journal, 2022, ISSN 1521-3765
Wydawca: Wiley
DOI: 10.1002/chem.202200164

Immobilized Eosin Y for the photocatalytic oxidation of tetrahydroisoquinolines in flow

Autorzy: F. Herbrik, S. Rossi, M. Sanz, A. Puglisi, M. Benaglia
Opublikowane w: ChemCatChem, 2022, ISSN 1867-3899
Wydawca: WILEY
DOI: 10.1002/cctc.202200461

Ammonia–Borane-Mediated Reduction of Nitroalkenes

Autorzy: Maurizio Benaglia, Chiara Faverio, Monica Fiorenza Boselli, Laura Raimondi
Opublikowane w: SynOpen, Numer 04/04, 2020, Strona(/y) 116-122, ISSN 2509-9396
Wydawca: Thieme
DOI: 10.1055/s-0040-1705980

Electrochemical Organic Synthesis of Electron-Rich Biaryl Scaffolds: An Update

Autorzy: F. Medici, S. Resta, A. Puglisi, S. Rossi, L. Raimondi. M. Benaglia
Opublikowane w: Molecules, 2021, Strona(/y) 6968, ISSN 1420-3049
Wydawca: Multidisciplinary Digital Publishing Institute (MDPI)
DOI: 10.3390/molecules26226968

Eosin Y: Homogeneous Photocatalytic In-Flow Reactions and Solid-Supported Catalysts for In-Batch Synthetic Transformations

Autorzy: Fabian Herbrik, Patricia Camarero González, Milena Krstic, Alessandra Puglisi, Maurizio Benaglia, Miguel A. Sanz, Sergio Rossi
Opublikowane w: Applied Sciences, Numer 10/16, 2020, Strona(/y) 5596, ISSN 2076-3417
Wydawca: MDPI
DOI: 10.3390/app10165596