Méthodologie, Synthèse et Molécules Thérapeutiques
Publications de l'équipe
2024
Ferrocene-Mediated Electrochemical Polycyclization of Malonates. A. Lefevre, R. Guillot, C. Kouklovsky, G. Vincent, Org. Lett., 2024
Regio- and Chemoselective Double Allylic Substitution of Alkenyl vic-Diols. B. Chen, L. Pagès, R. Dollet, C. Kouklovsky, S. Prévost, A. De La Torre, Org. Lett., 2024, 26, 2393-2397
Total Synthesis of Mavacuran Alkaloids via Bioinspired and Non-Bioinspired Strategies. C. Kouklovsky, E. Poupon, L. Evanno, G. Vincent, Synlett, 2024, 35, 521-534
2023
Natural Product Synthesis: The Endless Quest for Unreachable Perfection. N. Fay, C. Kouklovsky, A. De La Torre, ACS Org. Inorg. Au, 2023, 3, 350-363
Total Synthesis of Lucidumone: Attempted Shortcuts, Dead Ends and Lessons Learnt. G. Huang, A. Laporte, L. Pagès, C. Kouklovsky, A. De La Torre, Synthesis, 2023, 55, A-H
Rapid Formation of Intramolecular Disulfide Bridges using Light: An Efficient Method to Control the Conformation and Function of Bioactive Peptides. F. He, Y. Chai, Z. Zeng, F. Lu, H. Chen, J. Zhu, Y. Fang, K. Cheng, E. Miclet, V. Alezra, Y. Wan, J. Am. Chem. Soc., 2023, 145, 22639-22648
Retro-[4+2]/Intramolecular Diels–Alder Cascade Allows a Concise Total Synthesis of Lucidumone. G. Huang, C. Kouklovsky, A. De La Torre, Synlett, 2023, 34, 1195-1199
Functional and structural insights into human N-deacetylase/N-sulfotransferase activities. S. D. Vallet, T. Annaval, R. R. Vivès, J. Hénault, C. Le Narvor, D. Bonnaffé, B. Priem, R. Wild, H. Lortat-Jacob, Proteoglycan Research, 2023, 1, e8
Benzylic C-H Arylation with Dicyanoarenes via Convergent Paired Electrolysis. S. Tang, G. Vincent, Green Chem., 2023, 25, 5483–5488
Diversity in the Synthesis of Functionalized Cyclohexene Oxide Derivatives by a Cycloaddition–Fragmentation Sequence from Benzene Oxide. F. Rambaud, R. Guillot, V. Alezra, C. Kouklovsky, J. Org. Chem., 2023, 88, 7152-7161
Using the Noncanonical Metallo-Amino Acid [Cu(II)(2,2′-Bipyridin-5-yl)]-alanine to Study the Structures of Proteins. L. C. Tabares, D. T. Daniel, J. L. Vasquez-Ibar, C. Kouklovsky, V. Alezra, S. Un, J. Phys. Chem. Lett., 2023, 14, 3368-3375
Collective Total Synthesis of Mavacuran Alkaloids through Intermolecular 1,4-Addition of an Organolithium Reagent. A. Mauger, M. Jarret, A. Tap, R. Perrin, R. Guillot, C. Kouklovsky, V. Gandon, G. Vincent, Angew. Chem. Int. Ed., 2023, 62, e202302461
2022
Customized Reversible Stapling for Selective Delivery of Bioactive Peptides. Z. Zeng, J. Zhu, X. Deng, H. Chen, Y. Jin, E. Miclet, V. Alezra, Y. Wan, J. Am. Chem. Soc., 2022, 144, 23614-23621
Total synthesis of grayanane natural products. N. Fay, R. Blieck, C. Kouklovsky, A. De La Torre, Beilstein J. Org. Chem., 2022, 18, 1707-1719
Structure of the human heparan sulfate polymerase complex EXT1-EXT2. F. Leisico, J. Omeiri, C. Le Narvor, J. Beaudouin, M. Hons, D. Fenel, G. Schoehn, Y. Couté, D. Bonnaffé, R. Sadir, H. Lortat-Jacob, R. Wild, Nat Commun, 2022, 13, 7110
1,2-Boronate Rearrangement: An Efficient Tool for the Opening, Functionalization and Formation of Strained Cycles. R. Blieck, A. De La Torre, Eur. J. Org. Chem., 2022, e202200920
Diastereo- and Enantioselective Inverse-Electron-Demand Diels–Alder Cycloaddition between 2-Pyrones and Acyclic Enol Ethers. G. Huang, R. Guillot, C. Kouklovsky, B. Maryasin, A. De La Torre, Angew. Chem. Int. Ed., 2022, 61, e202208185
Gram-Scale Enantioselective Synthesis of (+)-Lucidumone. G. Huang, C. Kouklovsky, A. De La Torre, J. Am. Chem. Soc., 2022, 144, 17803-17807
Preparation of an advanced intermediate for the synthesis of leustroducsins and phoslactomycins by heterocycloaddition. A. Rousseau, G. Vincent, C. Kouklovsky, Beilstein J. Org. Chem., 2022, 18, 1385-1395
Total Synthesis of Ophiorrhine A, G and Ophiorrhiside E Featuring a Bioinspired Intramolecular Diels-Alder Cycloaddition. W. Cao, Y. Dou, C. Kouklovsky, G. Vincent, Angew. Chem. Int. Ed., 2022, 61, e202209135
Unbiased C3-Electrophilic Indoles: Triflic Acid Mediated C3-Regioselective Hydroarylation of N-H Indoles. N. Sabat, W. Zhou, V. Gandon, X. Guinchard, G. Vincent, Angewandte Chemie-International Edition, 2022, 61, e202204400
Cerium(IV)-Mediated Carbon-Carbon Bond Formation for the Synthesis of Spirodienone Lactams. P. Adler, V. Perez, L. Roupnel, A. Fadel, N. Rabasso, Eur. J. Org. Chem., 2022, e202200646
Electrochemical Benzylic C–H Functionalization with Isocyanides. S. Tang, R. Guillot, L. Grimaud, M. R. Vitale, G. Vincent, Org. Lett., 2022, 24, 2125-2130
Regioselective Reductive Opening of Benzylidene Acetals with Dichlorophenylborane/Triethylsilane: Previously Unreported Side Reactions and How to Prevent Them. J. Hénault, P. Quellier, M. Mock-Joubert, C. Le Narvor, A. Alix, D. Bonnaffé, J. Org. Chem., 2022, 87, 963-973
Discrimination of deletion to point cytokine mutants based on an array of cross-reactive receptors mimicking protein recognition by heparan sulfate. M. Genuia, L.-A. Garçon, Y. N. Sergeeva, B. Musnier, A. Buhot, M. Billon, E. Gout, R. Sadir, H. Lortat-Jacob, C. Le Narvor, D. Bonnaffé, T. Livache, Y. Hou, Analytical and Bioanalytical Chemistry, 2022, 414, 551-559
2021
Anticipate, Target and Characterize: MS²-anticipated C-glycosylflavones from Erythrococca anomala. T. Kouamé, T. Okpekon, N. F. Bony, S. Ferron, D. Bonnaffé, J. Vanheuverzwijn, Z. Zhou, V. Fontaine, A. D. N’Tamon, J.-F. Gallard, K. Leblanc, J.-C. Jullian, C. Miel, P. Champy, M. A. Beniddir, P. Le Pogam, Planta Medica International Open, 2021, 8, e131-e142
Enantioselective Au(I)-catalyzed dearomatization of 1-naphthols with allenamides through Tethered Counterion-Directed Catalysis. Y. Yu, Z. Zhang, A. Voituriez, N. Rabasso, G. Frison, A. Marinetti, X. Guinchard, Chem. Commun., 2021, 57, 10779-10782
Polymyxin B-inspired non-hemolytic tyrocidine A analogues with significantly enhanced activity against gram-negative bacteria: How cationicity impacts cell specificity and antibacterial mechanism. J. Zhu, C. Hu, Z. Zeng, X. Deng, L. Zeng, S. Xie, Y. Fang, Y. Jin, V. Alezra, Y. Wan, European Journal of Medicinal Chemistry, 2021, 221, 113488
Highly stereoselective aldol reactions by Memory of Chirality: synthesis of quaternary β-hydroxy α-amino acids. L. Roupnel, R. Guillot, D. Gori, B. Viswambharan, C. Kouklovsky, V. Alezra, Helv. Chim. Act., 2021, 104, e2100127
Synthesis of a Seco iso-Secologanin Aglycone Analogue of Interest toward Secoiridoids and Monoterpene Indole Alkaloids. H. Abou-Hamdan, R. Guillot, C. Kouklovsky, G. Vincent, J. Org. Chem., 2021, 86, 9244-9252
Inverse‐Electron‐Demand Diels–Alder Reactions of 2‐Pyrones: Bridged Lactones and Beyond. G. Huang, C. Kouklovsky, A. De La Torre, Chemistry - A European Journal, 2021, 27, 4760-4788
The chemistry of mavacurane alkaloids: a rich source of bis-indole alkaloids. A. Mauger, M. Jarret, C. Kouklovsky, E. Poupon, L. Evanno, G. Vincent, Nat. Prod. Rep., 2021, 38, 1852-1886
Bioinspired Early Divergent Oxidative Cyclizations toward Pleiocarpamine, Talbotine, and Strictamine. M. Jarret, H. Abou-Hamdan, C. Kouklovsky, E. Poupon, L. Evanno, G. Vincent, Org. Lett., 2021, 23, 1355-1360
Gramicidin-S-Inspired Cyclopeptidomimetics as Potent Membrane-Active Bactericidal Agents with Therapeutic Potential. C. Hu, Q. Wen, S. Huang, S. Xie, Y. Fang, Y. Jin, R. Campagne, V. Alezra, E. Miclet, J. Zhu, Y. Wan, ChemMedChem, 2021, 16, 368-376
Natural products originated from the oxidative coupling of tyrosine and tryptophan: biosynthesis and bioinspired synthesis. S. Tang, G. Vincent, Chem. Eur. J., 2021, 27, 2612-2622
2020
Development of Therapeutic Gramicidin S Analogues Bearing Plastic β,γ-Diamino Acids. Q. Guan, K. Chen, Q. Chen, J. Hu, K. Cheng, C. Hu, J. Zhu, Y. Jin, E. Miclet, V. Alezra, Y. Wan, ChemMedChem, 2020, 15, 1089-1100
The Pivotal Role of N-O bonds in the Synthesis of Natural Products: A mini-review. C. Kouklovsky, Vietnam J. Chem., 2020, 58, 20-28
Bioinspired Divergent Oxidative Cyclizations of Geissoschizine: Total Synthesis of (–)‐17‐nor‐Excelsinidine, (+)‐16‐epi‐Pleiocarpamine, (+)‐16‐Hydroxymethyl‐Pleiocarpamine and (+)‐Taberdivarine H. M. Jarret, A. Tap, V. Turpin, N. Denizot, C. Kouklovsky, E. Poupon, L. Evanno, G. Vincent, Eur. J. Org. Chem., 2020, 6340-6351
Bioinspired Divergent Oxidative Cyclization from Strictosidine and Vincoside Derivatives: Second Generation Total Synthesis of Cymoside and Access to an Original Hexacyclic‐Fused Furo[3,2‐b]indoline. Y. Dou, C. Kouklovsky, G. Vincent, Chem. Eur. J., 2020, 26, 17190-17194
Dearomatization Reactions of Indoles to Access 3D Indoline Structures. H. Abou-Hamdan, C. Kouklovsky, G. Vincent, Synlett, 2020, 31, 1775-1788
Electrochemical Reduction of α-Amino Allenylphosphonates to α-Amino Allylphosphonates. P. Adler, P. De Oliveira, N. Rabasso, Eur. J. Org. Chem., 2020, 3918-3925
Electrochemical dearomative dihydroxylation and hydroxycyclization of indoles. J. Wu, R. Guillot, C. Kouklovsky, G. Vincent, Adv. Synth. Catal., 2020, 362, 1712-1719
Electrochemical synthesis of 3a-bromofuranoindolines and 3a-bromopyrroloindolines mediated by MgBr2. J. Wu, H. Abou-Hamdan, R. Guillot, C. Kouklovsky, G. Vincent, Chem. Commun., 2020, 56, 1713-1716
Enantioselective Total Synthesis of Cymoside through a Bioinspired Oxidative Cyclization of a Strictosidine Derivative. Y. Dou, C. Kouklovsky, V. Gandon, G. Vincent, Angewandte Chemie-International Edition, 2020, 59, 1527-1531
2019
Unexpected dimerization of a tripeptide comprising a β,γ-diamino acid. Y. Wan, J.-P. Baltaze, C. Kouklovsky, E. Miclet, V. Alezra, Journal of Peptide Science, 2019, 25, e3143
Recent Advances in the Exploration of Therapeutic Analogues of Gramicidin S, an Old but Still Potent Antimicrobial Peptide. Q. Guan, S. Huang, Y. Jin, R. Campagne, V. Alezra, Y. Wan, J. Med. Chem., 2019, 62, 7603-7617
Copper-Catalyzed Phosphonylation/Trifluoromethylation of N-p-NO2-Benzoylacrylamides Coupled with Dearomatization and Denitration. J. Wu, D. Ma, G. Tang, Y. Zhao, Org. Lett., 2019, 21, 7674-7678
Dearomatization of 3‐Nitroindoles with Highly γ‐Functionalized Allenoates in Formal (3+2) Cycloadditions. L. Birbaum, L. Gillard, H. Gérard, H. Oulyadi, G. Vincent, X. Moreau, M. De Paolis, I. Chataigner, Chem. Eur. J., 2019, 25, 13688-13693
One-pot synthesis of a new generation of hybrid bisphosphonate polyoxometalate gold nanoparticles as antibiofilm agents. S. Tomane, E. López-Maya, S. Boujday, V. Humblot, J. Marrot, N. Rabasso, J. Castells-Gil, C. Sicard, A. Dolbecq, P. Mialane, A. Vallée, Nanoscale Adv., 2019, 1, 3400-3405
Bioinspired Oxidative Cyclization of the Geissoschizine Skeleton for Enantioselective Total Synthesis of Mavacuran Alkaloids. M. Jarret, V. Turpin, A. Tap, J.-F. Gallard, C. Kouklovsky, E. Poupon, G. Vincent, L. Evanno, Angewandte Chemie-International Edition, 2019, 58, 9861-9865
A Fused Hexacyclic Ring System: Diastereoselective Polycyclization of 2,4‐Dienals through an Interrupted iso‐Nazarov Reaction. A.-S. Marques, T. Duhail, J. Marrot, I. Chataigner, V. Coeffard, G. Vincent, X. Moreau, Angewandte Chemie-International Edition, 2019, 58, 9969-9973
Synthesis of 3,3-Spirocyclic 2-Phosphonoindolines via a Dearomative Addition of Phosphonyl Radicals to Indoles. D. Ryzhakov, M. Jarret, J.-P. Baltaze, R. Guillot, C. Kouklovsky, G. Vincent, Org. Lett., 2019, 21, 4986-4990
Substrate binding mode and catalytic mechanism of human heparan sulfate D-glucuronyl C5 epimerase. C. Debarnot, Y. R. Monneau, V. Roig-Zamboni, V. Delauzun, C. Le Narvor, E. Richard, J. Hénault, A. Goulet, F. Fadel, R. R. Vivès, B. Priem, D. Bonnaffé, H. Lortat-Jacob, Y. Bourne, Proc Natl Acad Sci USA, 2019, 116, 6760-6765
Electrochemical Dearomative 2,3-Difunctionalization of Indoles. J. Wu, Y. Dou, R. Guillot, C. Kouklovsky, G. Vincent, J. Am. Chem. Soc., 2019, 141, 2832-2837.
2018
Memory of Chirality in a Flow-Based System: Enantioselective Synthesis of Quaternary α-Amino Acids Using Flow Microreactors. A. Mambrini, D. Gori, C. Kouklovsky, H. Kim, J.-I. Yoshida, V. Alezra, European Journal of Organic Chemistry, 2018, 6754-6757
Oxidative coupling of enolates using memory of chirality: an original enantioselective synthesis of quaternary α-amino acid derivatives. A. Mambrini, D. Gori, R. Guillot, C. Kouklovsky, V. Alezra, Chem. Commun., 2018, 54, 12742-12745
Constrained Cyclic β,γ-Diamino Acids from Glutamic Acid: Synthesis of Both Diastereomers and Unexpected Kinetic Resolution. Y. Wan, N. Auberger, S. Thétiot-Laurent, F. Bouillère, A. Zulauf, J. He, S. Courtiol-Legourd, R. Guillot, C. Kouklovsky, S. Cote Des Combes, C. Pacaud, I. Devillers, V. Alezra, European Journal of Organic Chemistry, 2018, 329-340
N-Iodosuccinimide-Mediated Oxidative Coupling of Indoles and Phenols: A Synthetic Study toward the Benzofuroindoline Moiety of Bipleiophylline. N. Denizot, R. Guillot, C. Kouklovsky, G. Vincent, Synthesis, 2018, 50, 4823-4828
Combining Pure Shift And J-Edited Spectroscopies: A Strategy For Extracting Chemical Shifts And Scalar Couplings From Highly Crowded Proton Spectra Of Oligomeric Saccharides. D. Pitoux, Z. Hu, B. Plainchont, D. Merlet, J. Farjon, D. Bonnaffe, N. Giraud, Magn. Reson. Chem., 2018, 56, 954-962
Diastereoselective Synthesis of an Advanced Intermediate of Thapsigargin and Other 6,12-Guaianolides Using a RCEYM Strategy. M. Jouanneau, K. R. Bonepally, A. Jeuken, A. Tap, R. Guillot, J. Ardisson, J.-P. Férézou, J. Prunet, Org. Lett., 2018, 20, 2176-2180
Bioinspired Oxidative Cyclization of the Geissoschizine Skeleton for the Total Synthesis of (‐)‐17‐nor‐Excelsinidine. M. Jarret, A. Tap, C. Kouklovsky, E. Poupon, L. Evanno, G. Vincent, Angewandte Chemie-International Edition, 2018, 57, 12294-12298
Dearomative Diallylation of N-Acylindoles Mediated by FeCl3. J. Wu, R. K. Nandi, R. Guillot, C. Kouklovsky, G. Vincent, Org. Lett., 2018, 20, 1845-1848
Base mediated fragmentation of bicyclic dihydro-3,6-oxazines: transformation of nitroso Diels-Alder cycloadducts. R. Campagne, F. Schäkel, R. Guillot, V. Alezra, C. Kouklovsky, Org. Lett., 2018, 20, 1884-1887
β,γ-Diamino acids as building blocks for new analogues of Gramicidin S: synthesis and biological activity. Y. Wan, A. Stanovych, D. Gori, S. Zirah, C. Kouklovsky, V. Alezra, Eur. J. Med. Chem., 2018, 149, 122-128.
Divergent Oxidative Couplings between Indoles and 2,3-Dihydroxybenzoic Acid Derivatives for the Biomimetic Synthesis of Voacalgine A and Bipleiophylline. N. Denizot, D. Lachkar, C. Kouklovsky, E. Poupon, L. Evanno, G. Vincent, Synthesis, 2018, 50, 4229-4242
In Situ Generation of Cyclopentadienol Intermediates from 2,4-Dienals. Application to the Synthesis of Spirooxindoles via a Domino Polycyclization. A.-S. Marques, J. Marrot, I. Chataigner, V. Coeffard, G. Vincent, X. Moreau, Org. Lett., 2018, 20, 792-795
Triflic acid as an efficient Brønsted acid promoter for the Umpolung of N-Ac indoles in hydroarylation reactions. R. K. Nandi, A. Perez-Luna, D. Gori, R. Beaud, R. Guillot, C. Kouklovsky, V. Gandon, G. Vincent, Adv. Synth. Catal., 2018, 360, 161–172
Interfering peptides targeting protein–protein interactions: the next generation of drugs? H. Bruzzoni-Giovanelli, V. Alezra, N. Wolff, C.-Z. Dong, P. Tuffery, A. Rebollo, Drug Discovery Today, 2018, 23, 272-285
2017
A Versatile Electronic Tongue Based on Surface Plasmon Resonance Imaging and Cross-Reactive Sensor Arrays-A Mini-Review. L.-A. Garçon, M. Genua, Y.-J. Hou, R. Calemczuk, T. Livache, M. Billon, C. Le Narvor, D. Bonnaffé, H. Lortat-Jacob, Y. Hou, Sensors, 2017, 17, 1046
Radical-Mediated Dearomatization of Indoles with Sulfinate Reagents for the Synthesis of Fluorinated Spirocyclic Indolines. D. Ryzhakov, M. Jarret, R. Guillot, C. Kouklovsky, G. Vincent, Org. Lett, 2017, 19, 6336-6339
Expedient Approach to α,β-Unsaturated δ-Lactones via a Catalytic Asymmetric [2+2] Cycloaddition. C. Kouklovsky, A. Rousseau, M. Buchotte, R. Guillot, G. Vincent, Eur. J. Org. Chem., 2017, 6804-6810
Synthesis of N-Sulfonyl Ynamido-Phosphonates: Valuable Partners for Cycloadditions. V. Perez, A. Fadel, N. Rabasso, Synthesis, 2017, 49, 4035-4044
Frozen Chirality of Tertiary Aromatic Amides :Access to Enantioenriched Tertiary alpha-Amino Acid or Amino Alcohol without Chiral Reagent. T. T. Mai, B. Viswambharan, D. Gori, R. Guillot, J.-V. Naubron, C. Kouklovsky, V. Alezra, Chem. Eur. J., 2017, 23, 5787-5798
Revealing the Electrophilicity of N-Ac Indoles with FeCl3: a mechanistic study. R. Beaud, R. K. Nandi, A. Perez-Luna, R. Guillot, D. Gori, C. Kouklovsky, N. E. Ghermani, V. Gandon, G. Vincent, Chem. Commun., 2017, 53, 5834 - 5837
Evaluation of an NIS-Mediated Oxidative Cyclisation of Phenol-Containing N-Acyltryptamine Precursors towards Phalarine: Synthesis of 4′,5′-Dihydrospiro[indole-3,6′-[1,3]oxazine]s. T. Tomakinian, H. Abou Hamdan, N. Denizot, R. Guillot, J.-P. Baltaze, C. Kouklovsky, G. Vincent, Eur. J. Org. Chem., 2017, 19, 2757–2763
Unified biomimetic assembly of voacalgine A and bipleiophylline via divergent oxidative couplings. D. Lachkar, N. Denizot, G. Bernadat, K. Ahamada, M. A. Beniddir, V. Dumontet, J.-F. Gallard, R. Guillot, K. Leblanc, E. O. N'Nang, V. Turpin, C. Kouklovsky, E. Poupon, L. Evanno, G. Vincent, Nature Chemistry, 2017, 9, 793-798
From acyclic to cyclic α-amino vinylphosphonates by using ring-closing metathesis. P. Adler, A. Fadel, J. Prunet, N. Rabasso, Org. Biomol. Chem., 2017, 15, 387-395
2016
CD4-mimetic sulfopeptide conjugates display sub-nanomolar anti-HIV-1 activity and protect macaques against a SHIV162P3 vaginal challenge. K. K. Arien, F. Baleux, D. Desjardins, F. Porrot, Y.-M. Coic, J. Michiels, K. Bouchemal, D. Bonnaffe, T. Bruel, O. Schwartz, R. Le Grand, G. Vanham, N. Dereuddre-Bosquet, H. Lortat-Jacob, SCIENTIFIC REPORTS, 2016, 6
Iron-Mediated Domino Interrupted Iso-Nazarov/Dearomative (3 + 2)-Cycloaddition of Electrophilic Indoles. A.-S. Marques, V. Coeffard, I. Chataigner, G. Vincent, X. Moreau, Org. Lett., 2016, 18, 5296-5299
Recent Progress in Memory Of Chirality (MOC): An Advanced Chiral Pool. V. Alezra, T. Kawabata, Synthesis, 2016, 48, 2997-3016
Efficient synthesis of both diastereomers of β,γ-diamino acids from phenylalanine and tryptophan. N. Auberger, A. Stanovych, S. Thétiot-Laurent, R. Guillot, C. Kouklovsky, S. Cote Des Combes, C. Pacaud, I. Devillers, V. Alezra, Amino Acids, 2016, 48(9), 2237-2242
Synthesis of 3,3-Spiroindolines via FeCl3-Mediated Cyclization of Aryl- or Alkene-Containing 3-Substituted N-Ac Indoles. R. K. Nandi, R. Guillot, C. Kouklovsky, G. Vincent, Org. Lett., 2016, 18, 1716-1719
Synthesis of benzofuro[3,2-b]indoline amines via deamination-interrupted Fischer indolization and their unexpected reactivity towards nucleophiles. T. Tomakinian, R. Guillot, C. Kouklovsky, G. Vincent, Chem. Commun., 2016, 52, 5443-5446
Intermolecular dearomative C2-arylation of N-Ac indoles activated by FeCl3. R. K. Nandi, F. Ratsch, R. Beaud, R. Guillot, C. Kouklovsky, G. Vincent, Chem. Commun., 2016, 52, 5328-5331
Synthesis of 5-Phosphonoisoxazoline N-Oxides by Selective O-Alkylation of Nitronate Anions. V. Perez, N. Rabasso, A. Fadel, Eur. J. Org. Chem., 2016, 320-324
2015
Magnetic field dependence of spatial frequency encoding NMR as probed on an oligosaccharide. D. Pitoux, Z. Hu, B. Plainchont, D. Merlet, J. Farjon, D. Bonnaffe, N. Giraud, Magn. Reson. Chem., 2015, 53, 836-844
Connecting Tyrosine and Tryptophan Units of Diazonamide A and Azonazine by a Diastereodivergent Arylative Dearomatization. N. Denizot, R. Guillot, C. Kouklovsky, G. Vincent, Chem. Eur. J., 2015, 21, 18953-18956
Synthesis of 3-arylated indolines from dearomatization of indoles. N. Denizot, T. Tomakinian, R. Beaud, C. Kouklovsky, G. Vincent, Tetrahedron Lett., 2015, 56, 4413-4429
Investigation of the Synthesis of Benzofuroindolines from N-Hydroxyindoles: An O-Arylation/[3,3]-Sigmatropic Rearrangement Sequence. T. Tomakinian, C. Kouklovsky, G. Vincent, Synlett, 2015, 1269-1275
The quest of an oxidative coupling of phenols and indoles towards benzofuroindolines: a two stage approach. R. Beaud, T. Tomakinian, N. Denizot, A. Pouilhès, C. Kouklovsky, G. Vincent, Synlett, 2015, 432-435
Mild Cleavage of N–O Bond of 3,6-Dihydro-1,2-oxazines by Condensation of Aldehydes in Aqueous Media. G. Galvani, R. Lett, C. Kouklovsky, Synlett, 2015, 26, 1340-1344
Fully Resolved NMR Correlation Spectroscopy. D. Pitoux, B. Plainchont, D. Merlet, Z. Hu, D. Bonnaffé, J. Farjon, N. Giraud, Chemistry - A European Journal, 2015, 21, 9044-9047
Cerium(iv) ammonium nitrate mediated 5-endo-dig cyclization of α-amino allenylphosphonates to spirodienones. P. Adler, A. Fadel, N. Rabasso, Chem. Commun., 2015, 51, 3612-3615
2014
Landscapes of taste by a novel electronic tongue for the analysis of complex mixtures. L.-A. Garçon, Y. Hou, M. Genua, A. Buhot, R. Calemczuk, D. Bonnaffé, Y. Hou, T. Livache, Sensor Letters, 2014, 12, 1059-1064
Oxidative degradation of amino acids and aminophosphonic acids by 2,2-bipyridine complexes of Copper(II). J. S. Pap, N. El Bakkali-Tahéri, A. Fadel, S. Goger, D. Bogath, M. Molnar, M. Giorgi, G. Speier, A. J. Simaan, J. Kaizer, Eur. J. Inorg. Chem, 2014, 2829–2838
From Chitin to Bioactive Chitooligosaccharides and Conjugates: Access to Lipochitooligosaccharides and the TMG-chitotriomycin. G. Despras, A. Alix, D. Urban, B. Vauzeilles, J.-M. Beau, Angew. Chem. Int. Ed., 2014, 53, 11912-11916
Strategies for the synthesis of α- and β-amino vinylphosphonate. P. Adler, A. Fadel, N. Rabasso, Tetrahedron, 2014, 70, 4437-4456
Cyclopropanation of 1,2-dibromoethylphosphonate: a synthesis of β-aminocyclopropylphosphonic acid and derivatives. N. Rabasso, A. Fadel, Tetrahedron Lett., 2014, 55, 6068-6071
Repairing the Thiol-Ene Coupling Reaction. G. Povie, A.-T. Tran, D. Bonnaffe, J. Habegger, Z. Hu, C. Le Narvor, P. Renaud, ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2014, 53, 3894-3898
Characterization of Glycosaminoglycan (GAG) Sulfatases from the Human Gut Symbiont Bacteroides thetaiotaomicron Reveals the First GAG-specific Bacterial Endosulfatase. J. E. Ulmer, E. M. Vilen, R. B. Namburi, A. Benjdia, J. Beneteau, A. Malleron, D. Bonnaffe, P.-A. Driguez, K. Descroix, G. Lassalle, C. Le Narvor, C. Sandstrom, D. Spillmann, O. Berteau, JOURNAL OF BIOLOGICAL CHEMISTRY, 2014, 289, 24289-24303
Electronic Tongue Generating Continuous Recognition Patterns for Protein Analysis. Y. Hou, M. Genua, L.-A. Garcon, A. Buhot, R. Calemczuk, D. Bonnaffe, H. Lortat-Jacob, T. Livache, JOVE-JOURNAL OF VISUALIZED EXPERIMENTS, 2014
SPR imaging based electronic tongue via landscape images for complex mixture analysis. M. Genua, L.-A. Garcon, V. Mounier, H. Wehry, A. Buhot, M. Billon, R. Calemczuk, D. Bonnaffe, Y. Hou, T. Livache, TALANTA, 2014, 130, 49-54
Substrate Control in Enantioselective and Diastereoselective Aldol Reaction by Memory of Chirality: A Rapid Access to Enantiopure β-Hydroxy Quaternary α-Amino Acids. B. Viswambharan, D. Gori, R. Guillot, C. Kouklovsky, V. Alezra, Org. Lett., 2014, 16, 788-791
Regioselective Hydroarylation Reactions of C3 Electrophilic N-Acetylindoles Activated by FeCl3: An Entry to 3-(Hetero)arylindolines. R. Beaud, R. Guillot, C. Kouklovsky, G. Vincent, Chem. Eur. J., 2014, 20, 7492-7500
Direct Oxidative Coupling of N-Acetyl Indoles and Phenols for the Synthesis of Benzofuroindolines Related to Phalarine. T. Tomakinian, R. Guillot, C. Kouklovsky, G. Vincent, Angew. Chem. Int. Ed., 2014, 53, 11881-11885
Bioinspired Direct Access to Benzofuroindolines by Oxidative [3 + 2] Annulation of Phenols and Indoles. N. Denizot, A. Pouilhès, M. Cucca, R. Beaud, R. Guillot, C. Kouklovsky, G. Vincent, Org. Lett., 2014, 16, 5752-5755
β,γ-Diamino acid: an original building block for hybrid α/γ-peptide synthesis with extra hydrogen bond donating group. A. Stanovych, R. Guillot, C. Kouklovsky, E. Miclet, V. Alezra, Amino Acids, 2014, 46, 2753-2757
2013
Selective Reduction of Amino Allenephosphonates: Preparation of α-Amino Vinylphosphonates. P. Adler, F. Gomes, A. Fadel, N. Rabasso, Eur. J. Org. Chem., 2013, 7546-7555
p-Methoxybenzyl-N-phenyl-2,2,2-trifluoroacetimidate: a versatile reagent for mild acid catalyzed etherification. N. Barroca-Aubry, M. Benchekroun, F. Gomes, D. Bonnaffe, Tetrahedron Lett., 2013, 54, 5118-5121
2012
[2,3]-Sigmatropic Rearrangement of Ynamides: Preparation of α-Amino Allenephosphonates. F. Gomes, A. Fadel, N. Rabasso, J. Org. Chem., 2012, 77, 5439-5444
2011
Synthesis of an Enkephalin Analogue Containing an α,α-Disubstituted Heterocyclic Aminophosphonic Acid. N. Rabasso, A. Fadel, Phosphorus, Sulfur Silicon Relat. Elem., 2011, 186, 1811-1819
Highly Regio- and Stereoselective Nickel-Catalyzed Addition of Dialkyl Phosphites to Ynamides: an Efficient Synthesis of β-Aminovinylphosphonates. A. Fadel, F. Legrand, G. Evano, N. Rabasso, Ad. Synth. Catal., 2011, 353, 263-267
2010
Synthesis of new β- and γ-aminopyrrolidinephosphonates via 1,3-dipolar cycloaddition of substituted vinylphosphonates. N. Rabasso, A. Fadel, Tetrahedron Lett., 2010, 51, 60-63