Institut de Chimie Moléculaire et des Matériaux d'Orsay

Publications

 

35 Publications (31 articles scientifiques, 1 interview, 1 article de vulgarisation, 1 article pédagogique et 1 chapitre de livre)

  • h-index : 15
  • Citations : 606
  • Impact factor moyen (articles scientifiques hors acte/invitation) : 5.43 pour 28 publications
  • Impact factor moyen (articles scientifiques) : 5.03 pour 31 publications

 

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.

A Stable N-Heterocyclic Carbene Organocatalyst for Hydrogen/Deuterium Exchange Reactions between Pseudoacids and Deuterated Chloroform.

F. Perez, Y. Ren, T. Boddaert, J. Rodriguez, Y. Coquerel, J. Org. Chem. 2015, 80, 1092-1097


16.

Participation of Non-Aminoisobutyric Acid (Aib) Residues in the 310 Helical Conformation of Aib-Rich Foldamers: A solid State Study.

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.

Engineering the Structure of an N-Terminal beta-Turn To Maximize Screw-Sense Preference in Achiral Helical Peptide Chains.

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.

Conductors and insulators of screw-sense preference between helical oligo(aminoisobutyric acid) domains.

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

 

 

 

 

 

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.