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Publications

2021

Switching from single to simultaneous free radical and anionic polymerization with enamine-based organic electron donors https://doi.org/10.1002/anie.202106733

 Yuxi Zhao, Marion Rollet, Laurence Charles, Gabriel Canard, Didier Gigmes, Patrice Vanelle, Julie Broggi. Angew. Chem. Int. Ed., 2021, Accepted article

Generation of powerful organic electron donors by water-assisted decarboxylation of benzimidazolinium carboxylates https://doi.org/10.1039/D0QO01488E

 Guillaume Tintori, Arona Fall, Nadhrata Assani, Yuxi Zhao, David Bergé-lefranc, Sebastien Redon, Patrice Vanelle, Julie Broggi. J. Org. Org. Chem. Front., 2021, 8, 1197-1205

2020

Metal-Free Addition of Benzyl Halides to Aldehyde using Super Electron Donor: Acess to 3,4-diDydoisocoumarins and 1,2-Diarylethanols https://dx.doi.org/10.1021/acs.joc.0c02374

 Cédric Spitz, Mélanie Meutteudi, Guillaume Tintori, Julie Broggi, Thierry Terme and Patrice Vanelle. J. Org. Chem. 2020, 85, 15736-15742

Sequential regioselective Diorganochalcogenations of Imidazo[1,2-a]pyrimidines Using I2/H3PO4 in Dimethylsulfoxide https://doi.org/10.1021/acs.joc.9b02963

 Anne Roly Obah Kosso, Youssef Kabri, Julie Broggi, Sébastien Redon and Patrice Vanelle. J. Org. Chem. 2020

2019

Metal-Free ispo-Selenocyanation of Arylboronic Acids Using Malononitrile and Selenium Dioxide https://doi.org/10.1055/s-0039-1690013

 Anne Roly Obah Kosso, Julie Broggi, Sébastien Redon, Patrice Vanelle. Synthesis. 2019, 51, 3758-3764.

2018

Base-free generation of organic electron donors from air-stable precursors  https://doi.org/10.1002/anie.201713079

G. Tintori, P. Nabokoff, R. Buhaibeh, D. Bergé-Lefranc, S. Redon, J. Broggi, P. Vanelle. Angew. Chem. Int. Ed., 2018, 57, 3148-3153

Convenient and rapid synthesis of 3-selenocyanato-4H-chromen-4-ones https://doi.org/10.1055/s-0037-1609340

A. R. Obah Kosso, J. Broggi, S. Redon, P. Vanelle. Synlett. 2018, 29, 1215-1218.

untitled

2017

Easy and efficient selenocyanation of imidazoheterocycles using triselenodicyanide https://doi.org/10.1016/j.tetlet.2017.06.003

S. Redon, A. R. Obah Kosso, J. Broggi, P. Vanelle. Tetrahedron Lett. 2017, 58, 2771-2773.

2016

Polymerization Initiated by Organic Electron Donors  https://doi.org/10.1002/anie.201600327

J. Broggi, M. Rollet, J.L. Clément, G. Canard, T. Terme, D. Gigmes, P. Vanelle. Angew. Chem. Int. Ed. 2016, 55, 5994-5999.

Studies toward the oxidative and reductive activation of C-S bonds in 2′-S-aryl-2′-thiouridine derivatives https://doi.org/10.1016/j.tet.2016.02.063

R. Rayala , A. Giuglio-Tonolo,  J. Broggi, T. Terme, P. Vanelle, P. Theard, M. Médebielle, S. F. Wnuk. Tetrahedron, 2016, 72, 1969-1977.

2014

Organic Electron Donors as Powerful Single-Electron Transfer Reducing Agents in Organic Synthesis https://doi.org/10.1002/anie.201209060

J. Broggi, T. Terme, P. Vanelle, Angew. Chem., Int. Ed. 2014, 53, 384-413.

Synthesis and in vitro evaluation of 4-trichloromethylpyrrolo[1,2-a]quinoxalines as new antiplasmodial agents https://doi.org/10.1016/j.ejmech.2014.06.014

N. Primas, P. Suzanne, P. Verhaeghe, S. Hutter, C. Kieffer, M. Laget, A. Cohen, J. Broggi, , J. C. Lancelot, A. Lesnard, P. Dallemagne, P. Rathelot, S. Rault, P. Vanelle, N. Azas. Eur. J. Med. Chem. 2014, 83, 26-35.

2013

The Isolation of [Pd{OC(O)H}(H)(NHC)(PR3)] (NHC = N-Heterocyclic Carbene) and Its Role in Alkene and Alkyne Reductions Using Formic Acid https://doi.org/10.1021/ja311087c

J. Broggi, V. Jurčík, O. Songis, A. Poater, L. Cavallo, A. M. Z. Slawin, C. S. J. Cazin. J. Am. Chem. Soc. 2013, 135, 4588-4591.

2012

Coordinatively Unsaturated Ruthenium Complexes As Efficient Alkyne–Azide Cycloaddition Catalysts https://doi.org/10.1021/om2012425

M. Lamberti, G. C. Fortman, A. Poater, J. Broggi, A. M. Z. Slawin, L. Cavallo, S. P. Nolan. Organometallics, 2012, 31, 756-767.

2011

Novel Antiviral C5-Substituted Pyrimidine Acyclic Nucleoside Phosphonates Selected as Human Thymidylate Kinase Substrates https://doi.org/10.1021/jm1011462

D. Topalis, U. Pradère, V. Roy, C. Caillat, A. Azzouzi, J. Broggi, R. Snoeck, G. Andrei, J. Lin, S. Eriksson, J. A. C. Alexandre, C. El-Amri,  D. Deville-Bonne, P. Meyer, J. Balzarini, L. A. Agrofoglio. J. Med. Chem. 2011, 54, 222-232.

2010

The Influence of Phosphane Ligands on the Versatility of Ruthenium-Indenylidene Complexes in Metathesis https://doi.org/10.1002/chem.201000659

J. Broggi, C. A. Urbina-Blanco, H. Clavier, A. LeitgebC. Slugovc, A. M.Z. Slawin,  S. P. Nolan. Chem. Eur. J. 2010, 16, 9215-9225.

Ring-rearrangement metathesis (RRM) mediated by ruthenium-indenylidene complexes https://doi.org/10.1002/ejoc.200901316

H. Clavier, J. Broggi, S. P. Nolan. Eur. J. Org. Chem., 2010, 937-943.

2009

Click Azide-Alkyne Cycloaddition for the Synthesis of D-(-)-1,4-disubstituted-triazolo-carbanucleosides https://doi.org/10.1002/ejoc.200801124

J. Broggi, H. Kumamoto,  S. Berteina-Raboin, S. P. Nolan, L. A. Agrofoglio. Eur. J. Org. Chem. 2009, 1880-1888.

Synthesis of (±)-1,2,3-triazolo-3’-deoxy-4’-hydroxymethyl carbanucleosides via ‘click’ cycloaddition https://doi.org/10.1016/j.tet.2008.11.065Get

Julie. Broggi,, Nicolas. Joubert, S. Díez-González, S. Berteina-Raboin, T. Zevaco, S. P. Nolan,  L. A. Tetrahedron 2009, 65, 1162-1170.

2008

N-Heterocyclic Carbenes (NHCs) Containing NC-Palladacycle Complexes: Synthesis and Reactivity in Aryl Amination Reactions https://doi.org/10.1021/om8006689

J. Broggi, H. Clavier, S. P. Nolan. Organometallics 2008, 27, 5525-5531.

Study of copper(I) catalysts for the synthesis of carbanucleosides via azide-alkyne 1,3-dipolar cycloaddition DOI: 10.1055/s-2007-990943

J. Broggi, S. Díez-González, J. L. Petersen, S. Berteina-Raboin, Steven P. Nolan, L. A. Agrofoglio. Synthesis, 2008, 141-148.

Preparation of acyclo nucleoside phosphonate analogues based on cross-metathesis https://doi.org/10.1021/om8006689

H. Kumamoto, D. Topalis, J. Broggi, U. Pradère, V. Roy, S. Berteina-Raboin, S. P. Nolan, D. Deville-Bonne, G. Andrei, R. Snoeck, D. Garin, J. M. Crance, L. A. Agrofoglio. Tetrahedron 2008, 64, 3517-3526.

2007

Study of Different Copper (I) Catalysts for the  Click Chemistry  Approach to Carbanucleosides https://doi.org/10.1080/15257770701501492

J. Broggi, N. Joubert, V. Aucagne, T. Zevaco, S. Berteina-Raboin, S.P. Nolan,  L. A. Agrofoglio. Nucleosides, Nucleotides & Nucleic Acids, 2007, 26, 779-783

Alkyne-Azide Click Chemistry Mediated Carbanucleosides Synthesis  https://doi.org/10.1080/15257770701534139

J. Broggi, N. Joubert, V. Aucagne, S. Berteina-Raboin, S. Diez-Gonzalez, S. Nolan, D. Topalis, D. Deville-Bonne, J. Balzarini, J.Neyts, G. Andrei, R. Snoeck, L. A. Agrofoglio. Nucleosides, Nucleotides & Nucleic Acids, 2007, 26, 1391-1394.

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