1. Brom, J.; Maruani, A.; Turcaud, S.; Lajnef, S.; Peyrot, F.; Micouin, L.; Benedetti, E. “[2.2]Paracyclophane-based coumarins: effective organo-photocatalysts for light-induced desulfonylation processes” Org. Biomol. Chem. 2023, just accepted. DOI: 10.1039/D3OB01711G (Preprint ChemRxiv – DOI: 10.26434/chemrxiv-2023-n4ds3).
  2. Brom, J.; Maruani, A.; Micouin, L.; Benedetti, E. “Light-driven reductive cleavage of sulfonamides promoted by thiourea organophotosensitizers”. J. Org. Chem. 2023,  88, 5923. DOI: 10.1021/acs.joc.3c00296 (Preprint ChemRxiv – DOI: 10.26434/chemrxiv-2022-jvdqw)
  3. Fleurisson, C.; Graidia, N.; Foricher, Y.; Benedetti, E.; Micouin, L.;  “Intramolecular Buchwald-Hartwig N-Arylation of Bicyclic Hydrazines: Practical Access to Spiro[indoline-2,3′-piperidines]”  Org. Biomol. Chem. 2023, 21, 3542. DOI: 10.1039/D3OB00406F (Preprint ChemRxiv – DOI: 10.26434/chemrxiv-2022-rqsqc)
  4. Felder, S.; Delcourt, M.-L.; Rodríguez, R.; Favereau, L.; Jeanne Crassous, J.; Micouin, L.; Benedetti, E. “Compact CPL emitters based on a [2.2]paracyclophane scaffold: recent developments and future perspectives”, J. Mater. Chem. C 202311, 2053 DOI:
  1. S. Felder, C. Sagné, E. Benedetti, L. Micouin “Small-Molecule 3D Ligand for RNA Recognition: Tuning Selectivity through Scaffold Hopping” ACS Chemical Biology, 2022, 17, 3069. DOI:
  2. S. Felder, M.-L. Delcourt, M.H.E. Bousquet, D.  Jacquemin, R. Rodríguez, L. Favereau, J. Crassous, L. Micouin, E. Benedetti “Planar chiral analogues of PRODAN based on a [2.2]paracyclophane scaffold: Synthesis and photophysical studies”. J. Org. Chem. 2022, 87, 147-158 DOI:
  3. Bicyclic 5-5 systems with one ring junction nitrogen atom: Two extra heteroatoms 2:0 Benedetti, E.; Micouin, L. Reference Collection in Chemistry, Molecular Science and Chemical Engineering Wiley, 2022. Volume 11, pp 145-173. DOI:10.1016/B978-0-12-409547-2.14935-2 
  1. S. Wu, L.A. Galan, M. Roux, F. Riobe, B. Le Guennic, Y. Guyot, T. Le Bahers, L. Micouin, O. Maury, E. Benedetti “Tuning the excited state properties of [2.2]paracyclophane-based antennas to ensure efficient sensitization of lanthanide ions or singlet oxygen generation” Inorg. Chem. 2021, 60, 16194−16203. DOI:
  2. S. Felder, S. Wu, J. Brom, L. Micouin, E. Benedetti,  “Enantiopure planar chiral [2.2]paracyclophanes: Synthesis and applications in asymmetric organocatalysis” Chirality, 2021, 33, 506-527 DOI:
  3. S. Felder, L. Micouin, E. Benedetti “Para‐functionalization of N‐substituted 4‐amino[2.2]paracyclophanes by regioselective formylation” Eur. J. Org. Chem., 2021, 4015-4018. DOI:
  4. C. Fleurisson, E. Benedetti, L. Micouin Cyclic cis-1,3-Diamines Derived from Bicyclic Hydrazines: Synthesis and Applications Synlett 2021, 31, 858-874. DOI: 10.1055/s-0040-1707324
  1. C. Aubry, P. Clerici, C. Gerbaud, L. Micouin, J.-L. Pernodet, S. Lautru, “Revised structure of Anthelvencine A and characterization of the Anthelvencin Biosynthetic gene cluster”.  ACS Chem Biol. 2020, 15, 945-951.
  2. C. Fleurisson, E. Benedetti, L. Micouin” Cyclic cis-1,3-Diamines Derived from Bicyclic Hydrazines: Synthesis and Applications” Synlett published online. DOI: 10.1055/s-0040-1707324
  3. X. Chen, P. Coric, V. Larue, S. Turcaud, X. Wang, S. Nonin-Lecomte, S. Bouaziz “The HIV-1 maturation inhibitor, EP39, interferes with the dynamic helix-coil equilibrium of the CA-SP1 junction of Gag” Eur. J. Med. Chem.2020204, 112634 DOI:
  4. Bicyclic 5-5 systems with one ring junction nitrogen atom: Two extra heteroatoms 2:0 Benedetti, E.; Micouin, L. Reference Collection in Chemistry, Molecular Science and Chemical Engineering Wiley, 2020. DOI:10.1016/B978-0-12-409547-2.14935-2 
  1. M.-L.Delcourt, C. Reynaud, S. Turcaud, L. Favereau, J. Crassous, L. Micouin, E. Benedetti, 3D Coumarin Systems Based on [2.2]Paracyclophane: Synthesis, Spectroscopic Characterization, and Chiroptical Properties. J. Org. Chem. 2019, 84 , 888–899.
  2. M.-L. Delcourt, S. Felder, S. Turcaud, C. H. Pollok, C. Merten, L. Micouin, E. Benedetti,  Highly Enantioselective Asymmetric Transfer Hydrogenation: A Practical and Scalable Method To Efficiently Access Planar Chiral [2.2]Paracyclophanes. J. Org. Chem. 2019, 84 , 5369–5382.
  3. R. Piccardi, S. Turcaud, E. Benedetti, L. Micouin, Synthesis and Reactivity of Mixed Dimethylalkynylaluminum Reagents. Synthesis, 2019, 51 , 97–106. (Published as part of the 50 Years SYNTHESIS – Golden Anniversary Issue)
  4. T. Zhao, L. Micouin, R. Piccardi, Synthesis of organometallic compounds in Flow, Helv. Chim. Acta, 2019, accepted (Special Issue for the 60th anniversary of Pr. Philipe Reanud)
  1. M.-L. Delcourt, S. Simon, E. Benedetti, L.Micouin, Highly Enantioselective Desymmetrization of Centrosymmetric pseudo-para-Diformyl[2.2]paracyclophane via Asymmetric Transfer Hydrogenation ACS Catalysis, 2018, 8, 6612-6616
  2. T. Zhao, R. Piccardi, L. Micouin. Rapid and Effective Synthesis of α-Acyloxy-α-alkynyltrimethylsilanes Org. Lett., 2018,20, 5015-5018
  3. A. Blond, S. Turcaud, T. Lecourt, L. Micouin Diastereoselective Ring Homologation of Bicyclic Hydrazines: Access to Cis-1,3-Diaminocyclohexitols. ACS OMEGA 2018, 3, 15302–15307.
  1. E. Benedetti, M.-L. Delcourt, B. Gatin-Fraudet, S. Turcaud, L. Micouin, Synthesis and photophysical studies of through-space conjugated [2.2]paracyclophane-based naphthalene fluorophores RSC Advances, 2017, 7, 50472-50476.
  2. H. Guyon, F. Mavré, M. Catala, S. Turcaud, F. Brachet, B. Limoges, C. Tisné, L. Micouin Use of a redox probe for an electrochemical RNA–ligand binding assay in microliter droplets Chem. Commun., 2017, 53, 1140-1143
  3. A. Joosten, M. Boultadaki-Arapinis, V. Gandon, L. Micouin, T. Lecourt, Substitution of the Participating Group of Glycosyl Donors by a Halogen Atom: Influence on the Rearrangement of Transient Orthoesters Formed during Glycosylation Reactions J. Org. Chem. 2017, 82, 3291-3297
  4. P. Gordillo, P. Clerici, L. Micouin Modular access to N-substituted cis 5-amino-3-hydroxypiperidines J. Org. Chem. 2017, 82, 7689-7694.