Publications
Margaux Bossuat, Pauline Rullière, Nadège Preuilh, Antonio Peixoto, Etienne Joly, Jean-Guillaume Gomez, Maroua Bourkhis, Frédéric Rodriguez, Fernanda Gonçalves, Isabelle Fabing, Hafida Gaspard, Vania Bernardes-Génisson, Valérie Maraval, Stéphanie Ballereau, Remi Chauvin, Sébastien Britton, Yves Génisson J. Med. Chem. 2023, 66, 20, 13918: Phenyl dialkynylcarbinols, a Bioinspired Series of Synthetic Antitumor Acetylenic Lipids
P. Demange, E. Joly, J. Marcoux, P. R. Zanon, D. Listunov, P. Rullière, C. Barthes, C. Noirot, J.-B. Izquierdo, A. Rozié, K. Pradines, R. Hee, M. V. de Brito, M. Marcellin, R.-F. Serre, O. Bouchez, O. Burlet-Schiltz, M. C. F. Oliveira, S. Ballereau, V. Bernardes-Génisson, V. Maraval, P. Calsou, S. M. Hacker, Y. Génisson, R. Chauvin, S. Britton, eLife 2022, 11, e73913: SDR enzymes oxidize specific lipidic alkynylcarbinols into cytotoxic protein-reactive species
Communication highlighted in an editor article: Marine sponge chemical and synthetic derivatives hijack human enzyme to kill cells.
BRITTON Sébastien, BALLEREAU Stéphanie, CALSOU Patrick, CHAUVIN Rémi, RULLIERE Pauline, GASPARD Hafida, GENISSON Yves, LISTUNOV Dymytrii, MARAVAL Valérie. Brevet déposé au European Patent Office, Septembre 2021.
Rullière P. ; Lizeaux F. ; Joly E. ; Gaspard, H. ; Maraval, V. ; Chauvin R. ; Génisson Y. , J. Fr. Ukr. Chem. 2019, 7, 1–9 : Fluorinated analogues of lipidic dialkynylcarbinols pharmacophores:synthesis and bioactivity.
Rullière, P. ; Cannillo, A. ; Grisel, J. ; Cividino P.; Carret, S. ; Poisson, J.-F. Org. Lett. 2018, 20, 4558–4561 : Total Synthesis of Proteasome Inhibitor (−)-Omuralide through Asymmetric Ketene [2 + 2]-Cycloaddition.
Rullière, P. ; Benoit, G. ; Allouche, E. M. D. ; Charette, A. B. Angew. Chem. Int. Ed. 2018, 57, 5777–5782 : Safe and facile access to nonstabilized diazoalkanes using continuous flow technology.
Listunov D. ; Joly, E. ; Rullière, P. ; Gaspard, H. ; Bernardes-Génisson, V. ; Génisson, Y. ; Maraval, V. ; Chauvin, R. , Synthesis 2018, 50, 3114–3130 : From natural to artificial antitumor lipidic alkynylcarbinols: asymmetric synthesis,enzymatic resolution, and refined SARs.
Bourkhis, M. ; Gaspard, H. ; Rullière, P. ; de Almeida D. K. C. ; Listunov D. ; Joly, E. ; Abderrahim, R. ; de Mattos, M. C. ; de Oliveira, M. C. F. ; Maraval, V. ; Chauvin, R. ; Génisson, Y. Chem. Med. Chem. 2018, 13, 1124 : Skeletal optimization of cytotoxic lipidic dialkynylcarbinols.
Rullière, P. in Encyclopedia of Reagents for Organic Synthesis; John Wiley & Sons, Ltd Chichester, UK, 2017; pp 1–2 : N,N,S-Trimethyl-S-phenylsulfoxinium Tetrafluoroborate.
Rullière, P. in Encyclopedia of Reagents for Organic Synthesis; John Wiley & Sons, Ltd Chichester, UK, 2017; pp 1–3 : Methyl 3-Methoxyacrylate.
Rullière, P.; Grisel, J.; Poittevin, C.; Cividino, P.; Carret, S.; Poisson, J.-F. Org. Lett. 2016, 18, 2824–2827. : Thermal [2 + 2]-cycloaddition of ketenes with chiral enol ethers: route to densely substituted cyclobutanones.
Rullière, P.; Cyr, P.; Charette, A. B. Org. Lett 2016, 18, 1988–1991 : Difluorocarbene addition to alkenes and alkynes incontinuous flow.
Rullière, P. in Encyclopedia of Reagents for Organic Synthesis; John Wiley & Sons, Ltd Chichester, UK, 2016; pp 1–2 : 3-[(Methylnitrosamino)sulfonyl]benzoic Acid.
Rullière, P.; Carret, S.; Milet, A.; Poisson, J.-F. Chem. Eur. J. 2015, 21, 3876–3881 : Kinetic difference in the [2 + 2] cycloaddition of ketenes: an experimental and theoretical study.
Communication highlighted in a frontispiece, Chem. Eur. J. 2015, 21, DOI: 10.1002/chem.201581061.
Saitman, A.; Rulliere, P.; Sullivan, S. D. E.; Theodorakis, E. A. Org. Lett. 2011, 13, 5854–5857 : Total Synthesis of Norcembrenolide B and Scabrolide D.