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Pr.
 
Damien
 
BONNE

Portrait de Pr. Damien Bonne
Pr.
Damien
BONNE
AMU iSm2 Service 531
Campus Scientifique de St Jérôme
13397
Marseille cedex 20
Téléphone
Entrée
01/09/2007
Soutenance
06/11/2006
Directeur de thèse
Jieping Zhu
Parcours
2022 Promotion to Full professor
2015 Habilitation on 25th June 2015 (HDR, Associate professor).
2007 Nomination as “Maître de Conférences” (Assistant professor) at Aix-Marseille University with Pr. Jean Rodriguez.
2006/2007 Post-doctoral position at the university of de Bristol (UK, with Pr. V. K. Aggarwal). Palladium catalyzed synthesis of pyrrolidines from vinyl aziridines : application to the synthesis of allo-kaïnic acid.
2003/2006 Ph.D. at the « Institut de Chimie des Substances Naturelles (ICSN) » in Gif-sur-Yvette in the group of Dr. J. Zhu. AstraZeneca fellowship.
1999/2003 Engineering school (CPE Lyon).
1997/1999 DUT Chimie (Saint-Avold). 
Enseignements
Master degree : Lectures, practical chemistry exercises and tutorial courses in organic chemistry and retrosynthetic analysis.
Licence degree (MSc) : Lectures, tutorial courses and practical chemistry exercises in organic chemistry.
Thématiques

Enantioselective organocatalysis ; Multiple Bond-Forming Transformations ; Domino reactions ; Axial chirality ; Helical chirality ; medium-sized rings

Collaborations et groupes
  • Pr. Sébastien Thibaudeau, Institut de Chimie des Milieux et Matériaux de Poitiers, University of Poitiers.
  • Dr. Fabien Robert-Peillard, LCE, Marseille
  • Dr. Daniel Dauzonne, Institut Curie.
Responsabilités administratives
  • 2021-2024 : Treasurer of the board of the Organic Chemistry Division of the French Chemical Society
  • 2018-2021 : member of the board of the Organic Chemistry Division of the French Chemical Society
Publications (62)
Reference Résumé graphique HAL

Enantioselective Synthesis of Heteroatom‐Linked Non‐Biaryl Atropisomers

Abdelati Naghim, Jean Rodriguez, Olivier Chuzel, Gaëlle Chouraqui, Damien Bonne, Angewandte Chemie International Edition, 2024. <hal-04616856>

Padlocking dihydrofurannulation for the control of small degree of helicity built on a fused-tetracyclic core

Arthur Gaucherand, Expédite Yen-Pon, Diego García-López, Jean-Valère Naubron, Sara Chentouf, Michel Giorgi, Stéphane Humbel, Marion Jean, Jean Rodriguez, Damien Bonne, Chemical Science, 2024, 15, 7300 - 7307. <hal-04616826>

Enantioselective Nucleophilic Vinylic Substitution (S N V) toward 3-Alkenyl-bisoxindoles Facilitated by C6′ Steric Bulk of Cinchona Alkaloid

Xingyue Wang, Guishun Bai, Ruoqi Liu, Xiaoli Zhu, Xinyi Ye, Tao Zhang, Kui Zhang, Damien Bonne, Jean Rodriguez, Hong Wang, Xiaoze Bao, Organic Letters, 2023, 25, 5941-5945. <hal-04260573>

Enantioselective Organocatalysis and Superacid Activation: Challenges and Opportunities

Bastien Michelet, Agnès Martin-Mingot, Jean Rodriguez, Sébastien Thibaudeau, Damien Bonne, Chemistry - A European Journal, 2023, 29, e202300440. <hal-04047011>

Basicity‐Controlled [3+2] Cyclization of 3‐Hydroxyquinolin‐ones and β‐Chlorinated Nitrostyrenes

Jiamin Wu, Fei Hu, Guishun Bai, Yang Yang, Damien Bonne, Jean Rodriguez, Congyong Yue, Hong Wang, Xiaoze Bao, European Journal of Organic Chemistry, 2023, 26, e202300218. <hal-04153501>

Determination of dissolved nickel in natural waters using a rapid microplate fluorescence assay method

Fabien Robert-Peillard, El Mountassir El Mouchtari, Damien Bonne, Stéphane Humbel, Jean-Luc Boudenne, Bruno Coulomb, Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy [1994-...], 2022, 275, 121170. <hal-03621175>

Hidden Heptacyclic Chiral N-Acyl Iminium Ions: a New Entry to Enantioenriched Polycyclic Azepanes and Azocanes by Superacid-Promoted Intramolecular Pictet-Spengler Reaction

Yasmin Reviriot, Bastien Michelet, Rodolphe Beaud, Agnès Martin-Mingot, Frédéric Guégan, Sébastien Thibaudeau, Jean Rodriguez, Damien Bonne, Chemistry - A European Journal, 2022, 28, e202200432. <hal-03769652>

Selecting one out of six stereoisomers

Damien Bonne, Jean Rodriguez, Nature Catalysis, 2021, 4, 451-452. <hal-03278289>

On the Enantioselective Phosphoric-Acid-Catalyzed Hantzsch Synthesis of Polyhydroquinolines

Ophélie Quinonero, Clément Lemaitre, Marion Jean, Nicolas Vanthuyne, Christian Roussel, Damien Bonne, Thierry Constantieux, Cyril Bressy, Xavier Bugaut, Jean Rodriguez, Organic Letters, 2021, 23, 3394-3398. <hal-03285117>

Sub-ppb mercury detection in real environmental samples with an improved Rhodamine-based detection system

Sukhdev Singh, Bruno Coulomb, Jean-Luc Boudenne, Damien Bonne, Frédéric Dumur, Bertrand Simon, F. Robert-Peillard, Talanta, 2021, 121909. <hal-03026250>

Pages

Ouvrages (3)
Reference Résumé graphique HAL

Stereoselective Multiple Bond-Forming Transformations in Organic Synthesis

Eds.: J. Rodriguez, D. Bonne, John Wiley & Sons, Inc., Hoboken, NJ, USA, 2015.

Jean Rodriguez, Damien Bonne. Stereoselective Multiple Bond-Forming Transformations in Organic Synthesis. John Wiley & Sons, 2015, 978-1-118-67271-6. ⟨hal-01323433⟩

1-Nitrocyclohexene

David Pierrot, Damien Bonne, Jean Rodriguez 2014, e-EROS Encyclopedia of Reagents for Organic Synthesis. 1–5.

Chapitres d'ouvrages (4)
Reference Résumé graphique HAL

Reactions Involving an alpha,beta-Unsaturated Compound as Electrophilic Component with the Michael Addition as the Key Step

J. Rodriguez, D. Bonne, Y. Coquerel, T. Constantieux, dans 'Multicomponent Reactions 2', 'Science of Synthesis Reference Library', T. J. J. Müller, Ed., Thieme, Stuttgart, 2013, Chap. 2.1.1, p. 1-36.

Stereoselective Multicomponent Reactions: from Simple 1,3-Dicarbonyls to Functionalized Chiral Heterocycles

D. Bonne, Y. Coquerel, T. Constantieux, J. Rodriguez in Targets in Heterocyclic Systems - Chemistry and Properties, Vol. 15, Eds.: O. A. Attanasi, D. Spinelli, Societa? Chimica Italiana, Roma, 2011, pp. 140-163. 

Utilisation des dérivés 1,3-dicarbonylés dans les réactions domino et multicomposé

Damien Bonne, Thierry Constantieux, Yoann Coquerel, Jean Rodriguez Techniques de l'Ingénieur 2010, CHV2210

Damien Bonne, Thierry Constantieux, Yoann Coquerel, Jean Rodriguez. Utilisation des dérivés 1,3-dicarbonylés dans les réactions domino et multicomposé. Ideas in Chemistry and Molecular Sciences: Advances in Synthetic Chemistry, pp.CHV2210, 2010. ⟨hal-00680619⟩