Publications
37 Publications (33 articles scientifiques, 1 interview, 1 article de vulgarisation, 1 article pédagogique et 1 chapitre de livre)
- h-index : 17
- Citations : 682
2024 :
37.
In Situ Generation of 1-Acetylpyrene as a Visible-Light Photocatalyst for the Thia-Paternò-Büchi Reaction. G. Cormier, C. Allain, T. Boddaert, Angew. Chem. Int. Ed. 2024, accepted
2023 :
36.
Functionalized alkylidenecyclobutanes from a cyclopent-2-enone substrate via a tandem photochemical transformation and an allylic substitution protocol. X. Yu, T. Boddaert, D. J. Aitken, Advanced Synthesis & Catalysis, 2023, 365, 4002-4007
2022 :
35.
Preparation of Thietane Derivatives through Domino Photochemical Norrish Type II/Thia-Paternò–Büchi Reactions. M. I. Lapuh, G. Cormier, S. Chergui, D. J. Aitken, T. Boddaert, Organic Letters, 2022, 24, 8375-8380
2021 :
34.
Photoactivatable Small-Molecule Inhibitors for Light-Controlled TAM Kinase Activity. J. Le Bescont, L. Mouawad, T. Boddaert, S. Bombard, S. Piguel, ChemPhotoChem, 2021, 5, 989-994
33.
Pyrrolidinyl peptide nucleic acids bearing hydroxy-modified cyclobutane building blocks: Synthesis and binding properties. B. Ditmangklo, W. Sittiwong, T. Boddaert, T. Vilaivan, D. J. Aitken, Biopolymers (Peptide Science), 2021, 112, e23459
2020 :
32.
Formation of tetrahydrothiophenes via a thia-Paternò-Büchi-initiated domino photochemical reaction. A. F. Kassir, A. F. Kassir, R. Guillot, R. Guillot, M.-C. Scherrmann, M.-C. Scherrmann, T. Boddaert, T. Boddaert, D. J. Aitken, D. J. Aitken, Org. Lett., 2020, 22, 8522-8527
31.
Young Career Focus. T. Boddaert, Synform, 2020, 3, A62-A64
2019 :
30.
Stereocontrolled Preparation of Diversely Trifunctionalized Cyclobutanes. Z. Chang, Z. Chang, R. Guillot, R. Guillot, T. Boddaert, T. Boddaert, D. J. Aitken, D. J. Aitken, J. Org. Chem., 2019, 84, 10518-10525
29.
Brønsted acid catalysed synthesis of 3-(2-alkoxyethyl)indoles from α‐arylaminocyclobutanones and alcohols. L. Serusi, M. Bonnans, A. Luridiana, F. Secci, P. Caboni, T. Boddaert, D. J. Aitken, A. Frongia, Advanced Synthesis & Catalysis, 2019, 361, 1908-1912
28.
A Selective Deprotection Strategy for the Construction of trans-2-Aminocyclopropanecarboxylic Acid Derived Peptides. T. Boddaert, J. E. Taylor, S. D. Bull, D. J. Aitken, Org. Lett., 2019, 21, 100-103
2018 :
27.
Acid-catalyzed synthesis of functionalized arylthio cyclopropane carbaldehydes and ketones. S. Porcu, S. Porcu, A. Luridiana, A. Luridiana, A. Martis, A. Martis, A. Frongia, A. Frongia, G. Sarais, G. Sarais, D. J. Aitken, D. J. Aitken, T. Boddaert, T. Boddaert, R. Guillot, R. Guillot, F. Secci, F. Secci, Chem. Commun., 2018, 54, 13547-13550
26.
Preparation of cyclobutene acetals and tricyclic oxetanes through photochemical tandem and cascade reactions. J. Buendia, J. Buendia, Z. Chang, Z. Chang, H. Eijsberg, H. Eijsberg, R. Guillot, R. Guillot, A. Frongia, A. Frongia, F. Secci, F. Secci, J. Xie, J. Xie, S. Robin, S. Robin, T. Boddaert, T. Boddaert, D. J. Aitken, D. J. Aitken, Angewandte Chemie International Edition, 2018, 57, 6592-6596
25.
Synthesis of sila or germa-analogue of Motesanib. T. Boddaert, O. Querolle, L. Meerpoel, P. Angibaud, J. Maddaluno, M. Durandetti, Heterocycles 2018, 97, 1210-1218
24.
Cooperative 5- and 10-membered ring interactions in the 10-helix folding of oxetin homo-oligomers. S. S. Ragab, S. S. Ragab, A. F. Kassir, A. F. Kassir, R. Guillot, R. Guillot, M.-C. Scherrmann, M.-C. Scherrmann, T. Boddaert, T. Boddaert, D. J. Aitken, D. J. Aitken, Chem. Commun., 2018, 54, 1968-1971
23.
A Photochemical Route to 3- and 4-Hydroxy Derivatives of 2-Aminocyclobutane-1-carboxylic Acid with an all-cis Geometry. Z. Chang, Z. Chang, F. Boyaud, F. Boyaud, R. Guillot, R. Guillot, T. Boddaert, T. Boddaert, D. J. Aitken, D. J. Aitken, Journal of Organic Chemistry, 2018, 83, 527-534
2017.
22.
Synthesis of 2,2-bis(pyridin-2-yl amino)cyclobutanols and their conversion into 5-(pyridin-2-ylamino)dihydrofuran-2(3H)-ones. L. Ghisu, L. Ghisu, N. Melis, N. Melis, F. Secci, F. Secci, P. Caboni, P. Caboni, M. Arca, M. Arca, R. Guillot, R. Guillot, T. Boddaert, T. Boddaert, D. J. Aitken, D. J. Aitken, A. Frongia, A. Frongia, Org. Biomol. Chem., 2017, 15, 9779-9784
21.
Stereoselective and regioselective pinacol-type rearrangement of a fused bicyclic oxetanol scaffold. N. Melis, N. Melis, A. Luridiana, A. Luridiana, R. Guillot, R. Guillot, F. Secci, F. Secci, A. Frongia, A. Frongia, T. Boddaert, T. Boddaert, D. J. Aitken, D. J. Aitken, European Journal of Organic Chemistry, 2017, 2017, Issue 39, 5896–5902
2016.
20.
Synthetic access to all four stereoisomers of oxetin. A. F. Kassir, A. F. Kassir, S. S. Ragab, S. S. Ragab, T. A. M. Nguyen, T. A. M. Nguyen, F. Charnay-Pouget, F. Charnay-Pouget, R. Guillot, R. Guillot, M.-C. Scherrmann, M.-C. Scherrmann, T. Boddaert, T. Boddaert, D. J. Aitken, D. J. Aitken, J. Org. Chem., 2016, 81, 9983-9991
2015.
19.
Synthesis of functionalized tryptamines by Bronsted acid catalysed cascade reactions. N. Melis, F. Secci, T. Boddaert, D. J. Aitken, A. Frongia, Chem. Commun., 2015, 51, 15272-15275
18.
Conformational preferences in the β-peptide oligomers of cis-2-amino-1-fluorocyclobutane-1-carboxylic acid. A. Hassoun, A. Hassoun, C. M. Grison, C. M. Grison, R. Guillot, R. Guillot, T. Boddaert, T. Boddaert, D. J. Aitken, D. J. Aitken, New J. Chem., 2015, 39, 3270-3279
17.
F. Perez, Y. Ren, T. Boddaert, J. Rodriguez, Y. Coquerel, J. Org. Chem. 2015, 80, 1092-1097
16.
S. Pike, T. Boddaert, J. Raftery, S. Webb, J. Clayden, New J. Chem. 2015, 39, 3288-3294
2014.
15.
Anionic Access to Silylated and Germylated Binuclear Heterocycles.T. Boddaert, C. François, L. Mistico, O. Querolle, L. Meerpoel, P. Angibaud, M. Durandetti, J. Maddaluno, Chem. Eur. J. 2014, 20, 10131-10139
14.
M. De Poli, L. Byrne, R. A. Brown, J. Sola, A. Castellanos, T. Boddaert, R. Wechsel, J. D. Beadle, J. Clayden, J. Org. Chem. 2014, 78, 4659-4675
13.
Foldamer-Mediated Remote Stereocontrol: >1,60 Asymmetric Induction.
L. Byrne, J. Solà, T. Boddaert, T. Marcelli, R. W. Adams, G. A. Morris, J. Clayden, Angew. Chem., Int. Ed. 2014, 55, 151-155
Avant ma nomination.
12.
Intramolecular Sila-Matteson Rearrangement: a General Access to New Silylated Heterocycles. C. François, T. Boddaert, M. Durandetti, O. Querolle, L. Van Hijfte, L. Meerpoel, P. Angibaud, J. Maddaluno, Org. Lett. 2012, 14, 2074-2077
11.
T. Boddaert, J. Solà, M. Helliwell, J. Clayden, Chem. Commun. 2012, 48, 3397-3399
10.
Combination of Rearrangement with Metallic and Organic Catalyses: a Step- and Atom-Economical Approach to α-Spirolactones and -lactams. T. Boddaert, Y. Coquerel, J. Rodriguez, Eur. J. Org. Chem. 2011, 5061-5070
9.
N-Heterocyclic Carbene-Catalyzed Michael Additions of 1,3-Dicarbonyl Compounds. T. Boddaert, Y. Coquerel, J. Rodriguez, Chem. Eur. J. 2011, 17, 2266-2271
8.
Expeditious Divergent Synthetic Approach to Polycyclic Terpene-like Molecules. T. Boddaert, Y. Coquerel, J. Rodriguez, Chem. Eur. J. 2011, 17, 2048-2051
7.
Organocatalytic Activity of N-Heterocyclic Carbenes in the Michael Addition of 1,3-Dicarbonyls. Application to a Stereoselective Spirocyclization Sequence: T. Boddaert, Y. Coquerel, J. Rodriguez, Adv. Synth. Catal. 2009, 351, 1744-1748
6.
Microwave-assisted Cross-Metathesis of Acrylonitrile.
T. Boddaert, Y. Coquerel, J. Rodriguez, C. R. Chimie, 2009, 12, 872-875
5.
Synthetic Studies Towards Guaianolide Sesquiterpene Lactones.
I. Reboul, T. Boddaert, Y. Coquerel, J. Rodriguez, Eur. J. Org. Chem., 2008, 5379-5382
4.
Reluctant Cross-Metathesis Reactions: a Highly Beneficial Effect of Microwave Irradiation.
A. Michaut, T. Boddaert, Y. Coquerel, J. Rodriguez, Synthesis, 2007, 18, 2867-2871
2018.
3.
Formation de liaisons Si-C pour la synthèse d'héytérocycles silylés : méthodologies et applications. M. Durandetti, T. Boddaert, Actualité Chimique, 2018, 434, 11-18.
2015.
2.
Démarche progressive vers l’apprentissage par projet dans le cadre d’une formation scientifique. C. Narce, F. Brouillard, J. Parmentier, M. Thomas, F. Bernard, A. Ozgumus, E. Blanc, S. Chaillou, E. Provost, T. Boddaert, 8ème colloque : Questions de pédagogie dans l’enseignement supérieur 2015, 229-235.
2010.
1.
Multiple Bond-Forming Transformations: the Key Concept towards Eco-Compatible Synthetic Organic Chemistry.Y. Coquerel, T. Boddaert, M. Presset, D. Mailhol, J. Rodriguez, in Ideas in Chemistry and Molecular Sciences, Vol.1 Advances in synthetic chemistry, Pignataro B. Ed.; Wiley-VCH, Weinheim, 2010.