Centre d’Élaboration de Matériaux et d’Etudes Structurales (UPR 8011)


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Claire KAMMERER

Assistant Professor, University Paul Sabatier, Toulouse

 

 

 

CEMES-CNRS (UPR 8011), Groupe NanoSciences
29 Rue J. Marvig, BP 94347
31055 Toulouse Cedex 4 (France)
Tel.: +33 (0)5 67 52 43 52
E-mail : kammerer[at]cemes.fr

 

Research Experience

Since 2012: Assistant Professor
Université Paul Sabatier and CEMES-CNRS, Toulouse (NanoSciences Group)
Keywords: molecular motors, synthetic organic chemistry, multistep synthesis, transition metal-catalyzed reactions

2009-2012: Post-doctoral fellow (Alexander von Humboldt fellowship)
Technische Universität München, Munich, Germany
Advisor: Prof. Thorsten Bach
Synthetic studies toward the total synthesis of pulvomycin
Total synthesis of bretonin B

2008: Short Term Scientific Mission (COST D40)
Technische Universität Dortmund, Dortmund, Germany
Advisor: Prof. Norbert Krause
Gold-catalyzed hydroalkylation of allenes

2005-2009: Ph.D. in Organic Chemistry
Université Pierre et Marie Curie, Paris
Advisors: Prof. Giovanni Poli, Prof. Guillaume Prestat
C-C bonds formation via palladium-, ruthenium-, and gold-catalyzed domino reactions and cycloisomerizations

2004: ERASMUS internship
Stockholm University, Stockholm, Sweden
Advisor: Prof. Jan-Erling Bäckvall
Biomimetic dihydroxylations of olefins with ionic liquid-immobilized catalytic systems

 

Education

2009: Ph.D. in Organic Chemistry, Université Pierre et Marie Curie, Paris
2005: Master of Sciences - Organic and bioorganic chemistry, Université Pierre et Marie Curie, Paris
2002-2006: Ecole Normale Supérieure, Paris

 

Teaching

L1: lectures and tutorials in organic chemistry, lectures and tutorials in kinetics
L2
: tutorials and lab courses in organic chemistry
M1
: lab courses in organic and organometallic chemistry
Agrégation de Chimie
: lessons and lab courses in organic chemistry

 

Administrative tasks

Since 2012: Erasmus coordinator for molecular chemistry at Université Paul Sabatier
2013-2015: Member of the Scientific Council of CEMES

 

Prizes and distinctions

2014: Thieme Chemistry Journals Award
2009: Laureate of a Alexander von Humboldt fellowship for postdoctoral researchers

 

Publications

[21] A chiral molecular propeller designed for unidirectional rotations on a surface
Zhang, Y.; Calupitan, J. P.; Rojas, T.; Tumbleson, R.; Erbland, G.; Kammerer, C.; Ajayi, T. M.; Wang, S.; Curtiss, L. A.; Ngo, A. T.; Ulloa, S. E.; Rapenne, G.; Hla, S. W. Nature Commun. 2019, 10, 3742. Download

[20] Biomimetic and technomimetic single molecular machines
Kammerer, C.; Erbland, G. Gisbert, Y.; Nishino, T.; Yasuhara, K.; Rapenne, G. Chem. Lett. 2019, 48, 299-308. Download Cover

[19] Surface manipulation of a curved polycyclic aromatic hydrocarbon-based nano-vehicle molecule equipped with triptycene wheels
Soe, W.-H.; Durand, C.; Guillermet, O.; Gauthier, S.; Jacquot de Rouville, H.-P.; Srivastava, S.; Kammerer, C.; Rapenne, G.; Joachim, C. Nanotechnology 2018, 29, 495401. Download

[18] Expedient Synthesis of Thioether-Functionalized Hydrotris(indazolyl)borate as an Anchoring Platform for Rotary Molecular Machines
Erbland, G.; Gisbert, Y.; Rapenne, G.; Kammerer, C. Eur. J. Org. Chem. 2018, 4731. Download

[17] From the Synthesis of Nanovehicles to Participation in the First Nanocar Race — View from the French Team
Jacquot de Rouville, H.-P.; Kammerer, C.; Rapenne, G. Molecules 2018, 23, 612. Download

[16] Rotative single molecular motors on metallic surfaces
Kammerer, C.; Rapenne, G. in Encyclopedia of interfacial chemistry: Surface Science and Electrochemistry, Ed. K. Wandelt, Elsevier, Amsterdam, 2018, vol. 4, pp 803-809. Download

[15] Les moteurs moléculaires
Sirven, A.M.; Kammerer, C.; Rapenne, G. L’Actualité Chimique 2017, 418-419, 17-24. Download

[14] Sequential Pd-catalyzed allylic alkylation / Ru-catalyzed ring-closing metathesis
Lorion, M. M.; Kammerer, C.; Prestat, G.; Poli, G. in Comprehensive Organic Chemistry Experiments for the Laboratory Classroom, Eds. Afonso, C. A. M.; Candeias, N. R.; Simão, D. P.; Trindade, A. F.; Coelho, J. A. S.; Tan, B.; Franzén R., The Royal Society of Chemistry, 2017, 5, 650-655. Download

[13] La NanoCar Race, première course internationale de molécule-voitures
Joachim, C.; Durand, C.; Launay, J.-P.; Rapenne, G.; Kammerer, C.; Jacquot de Rouville, H.-P.; Garbage, T.;Martrou, D.; Soe, W.-H.; Gauthier, S.; Bouju, X.; Lepriol, A.; Abeilhou, P.; Pertel, C.; Pettiti, L.; Fillon, J.-N.; Collard, C.; Prévôts, E. L’Actualité Chimique 2016, 411, I-XX. Download

[12] Scorpionate hydrotris(indazolyl)borate ligands as tripodal platforms for surface-mounted molecular gears and motors
Kammerer, C.; Rapenne, G. Eur. J. Inorg. Chem. 2016, 2214-2226. Download Cover

[11] Synthesis of functionalized mono-, bis-, and trisethynyltriptycenes for one-dimensional self-assembly on surfaces
Sirven, A. M.; Garbage, R.; Qiao, Y.; Kammerer, C.; Rapenne, G. Chem. Eur. J. 2015, 21, 15013-15019. Download

[10] Triptycene or subphthalocyanine wheels and polyaromatic hydrocarbon nanovehicles
Jacquot de Rouville, H.-P.; Garbage, R.; Sirven, A.M.; Kammerer, C.; Rapenne, G. in Single Molecular Machines and Motors, Ed. G. Rapenne, Springer, Berlin, 2015, 5, 65-79. Download

[9] Synthesis of γ-lactams and γ-lactones via intramolecular Pd-catalyzed allylic alkylations
Kammerer, C.; Prestat, G.; Madec, D.; Poli, G. Acc. Chem. Res. 2014, 47, 3439-3447. Download

[8] Total synthesis of (+)-bretonin B: Access to the (E,Z,E)-triene core by a late-stage Peterson elimination of a convergently assembled silyl ether
Neubauer, T.; Kammerer-Pentier, C.; Bach, T. Chem. Commun. 2012, 48, 11629-11631. Download

[7] Dual reactivity of O-α-allenyl esters under palladium(0) catalysis: From carbopalladation/allylic alkylation domino sequence to decarboxylative allenylation
Kammerer-Pentier, C.; Diez Martinez, A.; Oble, J.; Prestat, G.; Merino, P.; Poli, G. J. Organomet. Chem. 2012, 714, 53-59. Download

[6] Pd-catalyzed asymmetric synthesis of N-allenyl amides and their Au-catalyzed cycloisomerizative hydroalkylation: A new route toward enantioenriched pyrrolidones
Boutier, A.; Kammerer-Pentier, C.; Krause, N.; Prestat, G.; Poli, G. Chem. Eur. J. 2012, 18, 3840-3844. Download

[5] Selectivity in palladium-catalyzed allylic substitution
Poli, G.; Prestat, G.; Liron, F.; Kammerer-Pentier, C. Top. Organomet. Chem. 2012, 38, 1-64. Download

[4] Palladium-catalyzed domino carbopalladation / 5-exo-allylic amination of α-amino allenamides: An efficient entry to enantiopure imidazolidinones
Beccalli, E.M.; Broggini, G.; Clerici, F.; Galli, S.; Kammerer, C.; Rigamonti, M.; Sottocornola, S. Org. Lett. 2009, 11, 1563-1566. Download

[3] Phosphine-free palladium-catalyzed allene carbopalladation / allylic alkylation domino sequence: A new route to 4-(α-styryl) γ-lactams
Kammerer, C.; Prestat, G.; Madec, D.; Poli, G. Chem. Eur. J. 2009, 15, 4224-4227. Download

[2] New picropodophyllin analogs via palladium-catalyzed allylic alkylation - Hiyama cross-coupling sequences
Vitale, M.; Prestat, G.; Lopes, D.; Madec, D.; Kammerer, C.; Poli, G.; Girnita, L. J. Org. Chem. 2008, 73, 5795-5805. Download

[1] Allylic alkylation and ring-closing metathesis in sequence: A successful cohabitation of Pd and Ru
Kammerer, C.; Prestat, G.; Gaillard, T.; Madec, D.; Poli, G. Org. Lett. 2008, 10, 405-408. Download