S. Bourg

发表

A Restrained Molecular Dynamics Empirical Approach for Generating a Small Set of Structures Representative of the Internal Flexibility of a Receptor

C. Marot, Samia Aci-Sèche, L. Morin-Allory, 2009 .

Mining Chemical Libraries with "Screening Assistant 2"

Vincent Le Guilloux, Alban Arrault, Lionel Colliandre, 2012, J. Cheminformatics.

Palladium‐Catalyzed Regioselective C−H Arylation of 4‐Azaindazole at C3, C5 and C7 Positions

P. Bonnet, Samia Aci-Sèche, S. E. Kazzouli, 2021 .

Hybrid Silica Based Materials as New Solid Phase Extractants.

J. Moreau, S. Bourg, O. Conocar, 2000 .

Synthesis and biological evaluation of 2,3-bis(het)aryl-4-azaindole derivatives as protein kinase inhibitors

F. Saab, F. Schoentgen, C. Guillouzo, 2011 .

In vitro and in vivo biological evaluation of new 4,5-disubstituted 1,2,3-triazoles as cis-constrained analogs of combretastatin A4.

D. Scherman, D. Dauzonne, G. Chabot, 2012, European journal of medicinal chemistry.

Synthesis of dihydropyrimidine α,γ-diketobutanoic acid derivatives targeting HIV integrase.

Y. Pommier, R. Schinazi, P. Bonnet, 2015, European journal of medicinal chemistry.

Efficient synthesis and first regioselective C-3 direct arylation of imidazo[1,2-b]pyrazoles.

J. Leger, C. Jarry, P. Bernard, 2012, Chemistry.

Design, synthesis, and biological activity of pyridopyrimidine scaffolds as novel PI3K/mTOR dual inhibitors.

Lionel Colliandre, Stéphane Bourg, Mohamed Akssira, 2014, Journal of medicinal chemistry.

Electrophilic selenocyclization in 2-ene-1,5-diol systems: unexpected oxetane vs. tetrahydrofuran formation

P. D. Weghe, S. Bourg, J. Eustache, 2003 .

Synthesis and biological evaluation of new 3-(6-hydroxyindol-2-yl)-5-(Phenyl) pyridine or pyrazine V-Shaped molecules as kinase inhibitors and cytotoxic agents.

L. Meijer, O. Lozach, C. Guillouzo, 2011, European journal of medicinal chemistry.

First Palladium‐Catalyzed Direct Regioselective C‐5 (Het)Arylation of Mono‐ or Disubstituted Thiazolo[3,2‐b][1,2,4]triazoles

C. Jarry, S. Routier, G. Guillaumet, 2014 .

Novel tetrahydropyrido[1,2-a]isoindolone derivatives (valmerins): potent cyclin-dependent kinase/glycogen synthase kinase 3 inhibitors with antiproliferative activities and antitumor effects in human tumor xenografts.

L. Meijer, C. Guguen-Guillouzo, O. Lozach, 2012, Journal of medicinal chemistry.

Synthesis of chromeno[3,4-b]indoles as Lamellarin D analogues: a novel DYRK1A inhibitor class.

L. Meijer, O. Lozach, S. Routier, 2012, European journal of medicinal chemistry.

Novel optimization of valmerins (tetrahydropyrido[1,2-a]isoindolones) as potent dual CDK5/GSK3 inhibitors.

L. Meijer, P. Bonnet, C. Guguen-Guillouzo, 2016, European journal of medicinal chemistry.

Mixed Si/C/M/O ceramics from 2,5-disilahexane/metal carbonyl (MFe and Co)

B. Boury, R. Corriu, S. Bourg, 1998 .

New Stable Titanocene and Zirconocene Catalyst Precursors for Polysilane Synthesis via Dehydrocoupling of Hydrosilanes

R. Corriu, S. Bourg, Marcus Enders, 1995 .

Thermal conversion of organosilicon cobalt precursors to mixed Si/Co/C/O ceramics

B. Boury, R. Corriu, S. Bourg, 1998 .

Tailoring of Organically Modified Silicas for the Solid-Liquid Extraction of Actinides

J. Moreau, S. Bourg, O. Conocar, 2001 .

Synthesis of New Silicon−Cobalt Clusters

B. Boury, F. Carré, R. Corriu, 1998 .

An overview of solvent extraction processes developed in Europe for advanced nuclear fuel recycling, Part 2 — homogeneous recycling

C. Ekberg, M. Miguirditchian, A. Geist, 2021, Separation Science and Technology.

An overview of solvent extraction processes developed in Europe for advanced nuclear fuel recycling, part 1 — heterogeneous recycling

C. Ekberg, M. Miguirditchian, A. Geist, 2020, Separation Science and Technology.

The SACSESS Hydrometallurgy Domain — An Overview☆

Andreas Geist, Robin J. Taylor, Christian Ekberg, 2016 .

SACSESS – the EURATOM FP7 project on actinide separation from spent nuclear fuels

A. Geist, S. Bourg, J. Narbutt, 2015 .

ACSEPT-Partitioning technologies and actinide science: Towards pilot facilities in Europe

Robin J. Taylor, Christian Ekberg, Giuseppe Modolo, 2011 .

Homogenous recycling of transuranium elements from irradiated fast reactor fuel by the EURO-GANEX solvent extraction process

M. Miguirditchian, A. Geist, G. Modolo, 2019, Radiochimica Acta.

Europart. European Research Programme for Partitioning of Minor Actinides Within High Active Wastes Issuing from the Reprocessing of Spent Nuclear Fuels

Giuseppe Modolo, S. Bourg, Pascal Baron, 2006 .

Block-type HTGR spent fuel processing: CEA investigation program and initial results

S. Bourg, J. Lacquement, S. Grandjean, 2006 .

Cinchona-based zwitterionic stationary phases: Exploring retention and enantioseparation mechanisms in supercritical fluid chromatography with a fragmentation approach.

P. Bonnet, C. West, Martina Ferri, 2019, Journal of chromatography. A.

Automatic first-order multiplet analysis in liquid-state NMR

J. Nuzillard, S. Bourg, E. Prost, 2006 .

Synthesis and biological evaluation of enantiomerically pure cyclopropyl analogues of combretastatin A4.

J. Florent, G. Chabot, S. Bourg, 2013, Bioorganic & medicinal chemistry.

Synthesis and Structure–Activity Relationships of Constrained Heterocyclic Analogues of Combretastatin A4

J. Florent, L. Morin-Allory, J. Seguin, 2011, ChemMedChem.

Design, synthesis and antiproliferative activities of biarylolefins based on polyhydroxylated and carbohydrate scaffolds.

T. Cresteil, Geneviève Aubert, Y. Chapleur, 2011, European journal of medicinal chemistry.

In vitro and in vivo Biological Evaluation of New 4,5‐Disubstituted 1,2,3‐Triazoles as cis‐Constrained Analogues of Combretastatin A4.

D. Scherman, D. Dauzonne, G. Chabot, 2012 .

Synthesis and properties of 2'-O-neopentyl modified oligonucleotides.

Samia Aci-Sèche, U. Asseline, S. Bourg, 2013, Organic & biomolecular chemistry.

Advances in tetrahydropyrido[1,2-a]isoindolone (valmerins) series: Potent glycogen synthase kinase 3 and cyclin dependent kinase 5 inhibitors.

L. Meijer, P. Bonnet, C. Guguen-Guillouzo, 2015, European journal of medicinal chemistry.

Design, Synthesis and SAR in 2,4,7-Trisubstituted Pyrido[3,2-d]Pyrimidine Series as Novel PI3K/mTOR Inhibitors

P. Bonnet, R. Nehmé, P. Morin, 2021, Molecules.

Assessment of the environmental footprint of nuclear energy systems. Comparison between closed and open fuel cycles

Ch. Poinssot, S. Bourg, C. Rostaing, 2014 .

Comparative Assessment of Protein Kinase Inhibitors in Public Databases and in PKIDB

Stéphane Bourg, Christophe Meyer, Pascal Bonnet, 2020, Molecules.

Synthesis and optimization of an original V-shaped collection of 4-7-disubstituted pyrido[3,2-d]pyrimidines as CDK5 and DYRK1A inhibitors.

L. Meijer, P. Bonnet, O. Lozach, 2014, European journal of medicinal chemistry.

PKIDB: A Curated, Annotated and Updated Database of Protein Kinase Inhibitors in Clinical Trials

Stéphane Bourg, Christophe Meyer, Pascal Bonnet, 2018, Molecules.

Thiopurine Derivative-Induced Fpg/Nei DNA Glycosylase Inhibition: Structural, Dynamic and Functional Insights

Virginie Gaudon, B. Castaing, V. Aucagne, 2020, International journal of molecular sciences.

Visual Characterization and Diversity Quantification of Chemical Libraries: 1. Creation of Delimited Reference Chemical Subspaces

Vincent Le Guilloux, Lionel Colliandre, Stéphane Bourg, 2011, J. Chem. Inf. Model..

Improving the nuclear energy sustainability by decreasing its environmental footprint. Guidelines from life cycle assessment simulations

Ch. Poinssot, Bernard Boullis, S. Bourg, 2016 .

Assessment of the Anticipated Environmental Footprint of Future Nuclear Energy Systems. Evidence of the Beneficial Effect of Extensive Recycling

Christophe Poinssot, Jérôme Serp, Stéphane Bourg, 2017 .

Role of recycling in advanced nuclear fuel cycles

Ch. Poinssot, Bernard Boullis, S. Bourg, 2015 .

Extraction of plutonium and americium using silica hybrid materials

J. Moreau, S. Bourg, O. Conocar, 2007 .

VSPrep: A KNIME workflow for the preparation of molecular databases for virtual screening.

Stéphane Bourg, Pascal Bonnet, Jade Fogha, 2020, Current medicinal chemistry.

Mining collections of compounds with Screening Assistant 2

Vincent Le Guilloux, Alban Arrault, Lionel Colliandre, 2012, Journal of Cheminformatics.

Coordination Mode and Kinetic Behavior of the Tetracarbonatozirconate Ion

J. Nuzillard, L. Dupont, J. Angiboust, 1999 .

Development of actinide separation processes for future nuclear fuel cycles in Europe

G. Modolo, J. Glatz, S. Bourg, 2015 .

The Chemical Basis for Separating Recycling Materials by Pyro-Processes

S. Bourg, 2021 .

The evaluation of the pyrochemistry for the treatment of Gen IV nuclear fuels – Inert matrix chlorination studies in the gas phase or molten chloride salts

S. Bourg, J. Lacquement, F. Péron, 2007 .

Fr-PPIChem: An academic compound library dedicated to protein-protein interactions.

Olivier Sperandio, Maria A Miteva, Bruno O Villoutreix, 2020, ACS chemical biology.

Design and biological evaluation of substituted 5,7-dihydro-6H-indolo[2,3-c]quinolin-6-one as novel selective Haspin inhibitors

P. Bonnet, S. Ruchaud, S. Routier, 2022, Journal of enzyme inhibition and medicinal chemistry.

Synthesis of a 2-Indolylphosphonamide Derivative with Inhibitory Activity Against Yersiniabactin Biosynthesis.

M. Marahiel, M. Miethke, S. Bourg, 2007 .

Assessment of the Relative Environmental Footprint of Nuclear Energy and Its Fuel Cycle

C. Poinssot, S. Bourg, 2021 .

VSPrep: A General KNIME Workflow for the Preparation of Molecules for Virtual Screening

Stéphane Bourg, Pascal Bonnet, Samia Aci-Sèche, 2017, Molecular informatics.

Advanced Reprocessing Developments in Europe Status on European Projects ACSEPT and ACTINET-I3

C. Ekberg, A. Geist, C. Poinssot, 2012 .

A perspective on the sharing of docking data

A. D. de Brevern, P. Bonnet, Joseph Rebehmed, 2023, Data in brief.

Comprehensive Network Map of ADME‐Tox Databases

Stéphane Bourg, Philippe Vayer, Baptiste Canault, 2017, Molecular informatics.

In vitro and in vivo biological evaluation of new 4,5-disubstituted 1,2,3-triazoles as cis-constrained analogs of combretastatin A4.

D. Scherman, G. Chabot, S. Bourg, 2012, European journal of medicinal chemistry.

Synthesis and optimization of an original V-shaped collection of 4-7-disubstituted pyrido[3,2-d]pyrimidines as CDK5 and DYRK1A inhibitors.

L. Meijer, P. Bonnet, O. Lozach, 2014, European journal of medicinal chemistry.

A perspective on the sharing of docking data

P. Bonnet, Joseph Rebehmed, Samia Aci-Sèche, 2023, Data in brief.

Partitioning and transmutation strategy R&D for nuclear spent fuel: the SACSESS and GENIORS projects

A. Geist, S. Bourg, B. Hanson, 2020, EPJ Nuclear Sciences & Technologies.

Could spent nuclear fuel be considered as a non-conventional mine of critical raw materials?

C. Poinssot, S. Bourg, 2017 .

Synthesis of a 2-indolylphosphonamide derivative with inhibitory activity against yersiniabactin biosynthesis

M. Marahiel, M. Miethke, S. Bourg, 2007 .

Efficient synthesis and first regioselective C-3 direct arylation of imidazo[1,2-b]pyrazoles.

J. Leger, C. Jarry, P. Bernard, 2012, Chemistry.