Institut de Chimie Moléculaire et des Matériaux d'Orsay

Nicolas Rabasso

Build. 410, office 117 – MSMT – ICMMO
Université Paris-Saclay
Rue du doyen Georges Poitou
91405 Orsay Cedex

+33 1 69 15 32 39

Nicolas Rabasso studied at the University Pierre et Marie Curie (Paris, France) and obtained his Ph. D. in 2003 under the guidance of Prof. C. Agami and Prof. F. Couty. His doctoral research was focused on new methodologies for the enantioselective synthesis from four to eight membered ring nitrogen heterocycles. He then spent a year on a post-doctoral fellowship at Boston University (Massachusetts, USA) with Prof. J. A. Porco Jr. working on the natural product synthesis (EI-1941-1 & 2 and cytoskyrin A). In 2004, he obtained a position at the University Paris-Sud (Orsay, France) as Maître de Conférences. He got his habilitation in February 2011. His research interests include synthetic methodology, aminoacids and their incorporation into peptides and aminophosphonates.

Recent papers

Cerium(IV)-Mediated Carbon-Carbon Bond Formation for the Synthesis of Spirodienone Lactams. P. Adler, V. Perez, L. Roupnel, A. Fadel, N. Rabasso, Eur. J. Org. Chem., 2022, 2022, e202200646

Enantioselective Au(i)-catalyzed dearomatization of 1-naphthols with allenamides through Tethered Counterion-Directed Catalysis. Y. Yu, Z. Zhang, A. Voituriez, N. Rabasso, G. Frison, A. Marinetti, X. Guinchard, Chem. Commun., 2021, 57, 10779-10782

Electrochemical Reduction of α-Amino Allenylphosphonates to α-Amino Allylphosphonates. P. Adler, P. De Oliveira, N. Rabasso, Eur. J. Org. Chem., 2020, 3918-3925

One-pot synthesis of a new generation of hybrid bisphosphonate polyoxometalate gold nanoparticles as antibiofilm agents. S. Tomane, E. López-Maya, S. Boujday, V. Humblot, J. Marrot, N. Rabasso, J. Castells-Gil, C. Sicard, A. Dolbecq, P. Mialane, A. Vallée, Nanoscale Adv., 2019, 1, 3400-3405

Synthesis of N-Sulfonyl Ynamido-Phosphonates: Valuable Partners for Cycloadditions. V. Perez, A. Fadel, N. Rabasso, Synthesis, 2017, 49, 4035-4044

From acyclic to cyclic α-amino vinylphosphonates by using ring-closing metathesis. P. Adler, A. Fadel, J. Prunet, N. Rabasso, Org. Biomol. Chem., 2017, 15, 387-395

Synthesis of 5-Phosphonoisoxazoline N-Oxides by Selective O-Alkylation of Nitronate Anions. V. Perez, N. Rabasso, A. Fadel, Eur. J. Org. Chem., 2016, 320-324

Cerium(iv) ammonium nitrate mediated 5-endo-dig cyclization of α-amino allenylphosphonates to spirodienones. P. Adler, A. Fadel, N. Rabasso, Chem. Commun., 2015, 51, 3612-3615

Strategies for the synthesis of α- and β-amino vinylphosphonate. P. Adler, A. Fadel, N. Rabasso, Tetrahedron, 2014, 70, 4437-4456

Cyclopropanation of 1,2-dibromoethylphosphonate: a synthesis of β-aminocyclopropylphosphonic acid and derivatives. N. Rabasso, A. Fadel, Tetrahedron Lett., 2014, 55, 6068-6071