Expand Flow – Accessing new chemical space via a combined flash- and photochemical flow chemistry approach for the functionalisation and ring expansion of heterocycles

MSCA (Marie Skłodowska-Curie)HORIZON-TMA-MSCA-PF-EFID: 101106497
EC Contribution
€1,728
Consortium Size
1 orgs
Start Year
2023
Summary

With ever-increasing costs for the development of new drugs, the call for the development of more cost-effective and efficient methodologies to streamline the access to new drug candidates is imperative. To access new chemical space, the ring-distortion strategy – late-stage modification of rings to a variety of different functionalized cyclic and acyclic motifs – has proven a particularly successful approach. Recently, numerous ring-expansion and functionalisation protocols to cyclopentanones, tetralones, γ-functionalized butanones from cyclobutanols have been developed using classical batch processes. Despite the advances, the translation to pharmaceutically relevant applications is still outstanding; mainly due to three factors:1)The application of heterocycles in these protocols has been very limited or even impossible 2)The two-carbon ring expansion has only been successful on aryl-substituted analogues, yet not on alkene-substituted analogues &3)Scale-up to practical quantities is often difficult due to the requirement for conditions difficult to realise using batch processing. Expand Flow presents a multidisciplinary project that lies in the intersection of flash chemistry and synthetic photo-catalysis with microfluidic engineering and computational chemistry for the development of a selective, sustainable and applicable methodology for the ring deconstruction and functionalisation of heterocycles. Ultimately, its applicability to the pharmaceutical industry will be proven by the total synthesis of THC and its hitherto unexplored heterocyclic analogues.Overall, this project will add a valuable tool to the synthetic chemist’s repertoire for the rapid, environmentally-friendly and cost-effective development of new drug candidates by the versatile functionalisation of various heterocycles. This innovative approach will have a high scientific, technological and societal impact, reinforcing the European competitiveness in the development of life-saving drugs.

Consortium (1)

Project Results (12)

Source: CORDIS, the EU research results database.

Publications (9)
1‐Oxa‐2,6‐Diazaspiro[3.3]heptane as a New Potential Piperazine Bioisostere – Flow‐Assisted Preparation and Derivatisation by Strain‐Release of Azabicyclo[1.1.0]butanes
Advanced Synthesis & Catalysis· 2025DOI
Elena Graziano, Philipp Natho, Michael Andresini, Fabrizio Mastrolorito, Iktedar Mahdi, Ernesto Mesto, Marco Colella, Leonardo Degennaro, Orazio Nicolotti, Renzo Luisi
Azabicyclo[1.1.0]butyl‐Substituted Sulfonimidoyl Fluoride: Electrophilic Hub Bridging Late‐Stage Azetidine Incorporation with Sufex Chemistry
Advanced Synthesis & Catalysis· 2025DOI
Defne Serbetci, Philipp Natho, Ernesto Mesto, Emanuela Schingaro, Marco Colella, Renzo Luisi
Continuous Flow Decarboxylative Monofluoroalkylation Enabled by Photoredox Catalysis
JACS Au· 2025DOI
Francesco Pasca, Yuri Gelato, Michael Andresini, Defne Serbetci, Philipp Natho, Giuseppe Romanazzi, Leonardo Degennaro, Marco Colella, Renzo Luisi
Flow chemistry as green technology for the genesis and use of organometallic reagents in the synthesis of key building blocks and APIs – An update
Tetrahedron Green Chem· 2025DOI
Philipp Natho, Renzo Luisi
Generation and Use of Cyclopropenyllithium under Continuous Flow Conditions
Organic Letters· 2025DOI
Francesco Soddu, Iktedar Mahdi, Maria Chiara Cabua, Francesco Secci, Philipp Natho, Riccardo Tassoni, Paolo Dambruoso, Ernesto Mesto, Marco Colella, Renzo Luisi
Iodonitrene-Mediated Nitrogen Transfer to Alkenes for the Direct Synthesis of NH-Aziridines
Journal of the American Chemical Society· 2025DOI
Yuri Gelato, Laura Marraffa, Francesco Pasca, Philipp Natho, Giuseppe Romanazzi, Arianna Tota, Marco Colella, Renzo Luisi
Shifting Lithium Amide Reactivity to the Radical Domain: Regioselective Radical C−H Functionalization of 3‐Iodooxetane for the Synthesis of 1,5‐Dioxaspiro[2.3]hexanes
Angewandte Chemie International Edition· 2025DOI
Philipp Natho, Marco Colella, Annarita Vicenti, Giuseppe Romanazzi, Faizan Ullah, Nadeem S. Sheikh, Andrew J. P. White, Francesco Pasca, Renzo Luisi
Synthesis of Aza‐S(VI) Fluorides and Primary Sulfonimidamides from Sulfinylamines
Advanced Synthesis & Catalysis· 2025DOI
Michael Andresini, Laura Marraffa, Defne Şerbetçi, Philipp Natho, Marco Colella, Leonardo Degennaro, Renzo Luisi
Towards greener-by-design fine chemicals. Part 1: synthetic frontiers
Chemical Society Reviews· 2025DOI
Theodore A. Gazis, Jonas Wuyts, Areti Moutsiou, Giulio Volpin, Mark J. Ford, Rodolfo I. Teixeira, Katherine M. P. Wheelhouse, Philipp Natho, Polona Žnidaršič-Plazl, Sonja Jost, Renzo Luisi, Brahim Benyahia, Bert U. W. Maes, Gianvito Vilé
Deliverables (2)
Other Results (1)
Periodic Reporting for period 1 - Expand Flow (Expand Flow – Accessing new chemical space via a combined flash- and photochemical flow chemistry approach for the functionalisation and ring expansion of heterocycles)