Research areaOrganic Synthetic Method

Organic Synthetic Method at ICBMS focuses on the development of chemical transformations to either access molecules with targeted applications or to devellop inovative synthetic methods using rational approaches and designs. Our expertise include total synthesis, metal-based catalysis, fluorine chemistry, organo-catalysis, photo-redox and electro-chemistries, mechanistic investigation, modelling and applied theoretical chemistry and found applications in supramolecular chemistry, small molecule activation, biomass valorization, sensors and drug synthesis.

Research topics ICBMS expertises

Catalysis

Organic Synthetic Method

Mechanism / Reactivity

Organic Synthetic Method

Fluorine Chemistry

Organic Synthetic Method

Synthesis and Methodology applied to biomolecules

Organic Synthetic Method

Photochemistry, Electrochemistry

Organic Synthetic Method

Publications Find the most recent scientific contributions

From the RNA-Peptide World: Prebiotic reaction conditions compatible with lipid membranes for the formation of lipophilic random peptides in the presence of short oligonucleotides, and more

Augustin Lopez, Antoine Vauchez, Ghinwa Ajram, Anastasiia Shvetsova, Gabrielle Leveau, Michele Fiore, Peter Strazewski*

Life 2024, 14, 108

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Photoredox-Catalyzed α−C−H Monoalkylation of Symmetric Polyols in the Presence of CO2

Archer, Gaétan; Meyrelles, Ricardo; Eder, Isabel; Kovács, Nóra; Maryasin, Boris; Médebielle, Maurice; Merad, Jérémy

Angew. Chem. Int. Ed. 2024, e202315329

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Electroreductive Synthesis of Nickel(0) complexes

Rubel, Camille Z.; Cao, Yilin; Ewing, Tamara El-Hayek; Laudadio, Gabriele; Beutner, Gregory L.; Wisniewski, Steven R.; Wu, Xiangyu; Baran, Phil S.; Vantourout, Julien C.; Engle, Keary M.

Angew. Chem. Int. Ed. 2023, 136, 2, e202311557

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Synthetic outer membrane vesicles bearing Tn antigen

Carolina Chieffo, Arnaud Comte, Peter Strazewski and Michele Fiore*

European Journal of Organic Chemistry 2023, 26, e202300820

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Difluoromethoxylated Ketones as Building Blocks for the Synthesis of Challenging OCF2H-Bearing N-Heterocycles

A. Loison, G. Hanquet, F. Toulgoat, T. Billard, A. Panossian and F. R. Leroux

Eur. J. Org. Chem. 2023, 26, e202300695

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