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Gérard Audran - Publications

Affiliations: 
Institute of Molecular Science AIx-Marseille Universités, Marseille, Provence-Alpes-Côte d'Azur, France 
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42 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Albalat M, Audran G, Holzritter M, Marque SRA, Mellet P, Vanthuyne N, Voisin P. An enzymatic acetal/hemiacetal conversion for the physiological temperature activation of the alkoxyamine C–ON bond homolysis Organic Chemistry Frontiers. DOI: 10.1039/D0Qo00559B  0.306
2019 Audran G, Jacoutot S, Jugniot N, Marque SRA, Mellet P. Shifting-Nitroxides to Investigate Enzymatic Hydrolysis of Fatty Acids by Lipases Using Electron Paramagnetic Resonance in Turbid Media. Analytical Chemistry. PMID 31013060 DOI: 10.1021/Acs.Analchem.9B00561  0.319
2019 Yamasaki T, Buric D, Chacon C, Audran G, Braguer D, Marque SRA, Carré M, Brémond P. Chemical modifications of imidazole-containing alkoxyamines increase C-ON bond homolysis rate: Effects on their cytotoxic properties in glioblastoma cells. Bioorganic & Medicinal Chemistry. PMID 30975504 DOI: 10.1016/J.Bmc.2019.03.029  0.329
2019 Audran G, Bagryanskaya E, Bagryanskaya I, Edeleva M, Joly J, Marque SRA, Iurchenkova A, Kaletina P, Cherkasov S, Hai TT, Tretyakov E, Zhivetyeva S. How intramolecular coordination bonding (ICB) controls the homolysis of the C–ON bond in alkoxyamines Rsc Advances. 9: 25776-25789. DOI: 10.1039/C9Ra05334D  0.326
2019 Audran G, Bosco L, Brémond P, Jugniot N, Marque SRA, Massot P, Mellet P, Koumba TMM, Parzy E, Rivot A, Thiaudière E, Voisin P, Wedl C, Yamasaki T. Enzymatic triggering of C–ON bond homolysis of alkoxyamines Organic Chemistry Frontiers. 6: 3663-3672. DOI: 10.1039/C9Qo00899C  0.31
2018 Jugniot N, Duttagupta I, Rivot A, Massot P, Cardiet C, Pizzoccaro A, Jean M, Vanthuyne N, Franconi JM, Voisin P, Devouassoux G, Parzy E, Thiaudiere E, Marque SRA, Bentaher A, ... Audran G, et al. An elastase activity reporter for Electronic Paramagnetic Resonance (EPR) and Overhauser-enhanced Magnetic Resonance Imaging (OMRI) as a line-shifting nitroxide. Free Radical Biology & Medicine. 126: 101-112. PMID 30092349 DOI: 10.1016/J.Freeradbiomed.2018.08.006  0.678
2018 Duttagupta I, Jugniot N, Audran G, Franconi JM, Marque SRA, Massot P, Mellet P, Parzy E, Thiaudière E, Vanthuyne N. Selective On/Off-Nitroxides as Radical Probes to Investigate Non-radical Enzymatic Activity by Electron Paramagnetic Resonance. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29722459 DOI: 10.1002/Chem.201800866  0.686
2017 Audran G, Bikanga R, Brémond P, Edeleva M, Joly JP, Marque SRA, Nkolo P, Roubaud V. How intramolecular hydrogen bonding (IHB) controls the C-ON bond homolysis in alkoxyamines. Organic & Biomolecular Chemistry. 15: 8425-8439. PMID 28952643 DOI: 10.1039/C7Ob02223A  0.317
2017 Nkolo P, Audran G, Bikanga R, Brémond P, Marque SRA, Roubaud V. C-ON bond homolysis of alkoxyamines: when too high polarity is detrimental. Organic & Biomolecular Chemistry. 15: 6167-6176. PMID 28692104 DOI: 10.1039/C7Ob01312D  0.322
2017 Audran G, Bikanga R, Brémond P, Joly JP, Marque SRA, Nkolo P. Normal, Leveled, and Enhanced Steric Effects in Alkoxyamines Carrying a β-Phosphorylated Nitroxyl Fragment. The Journal of Organic Chemistry. 82: 5702-5709. PMID 28508644 DOI: 10.1021/Acs.Joc.7B00541  0.32
2016 Audran G, Bagryanskaya EG, Brémond P, Edeleva MV, Marque SRA, Parkhomenko DA, Rogozhnikova OY, Tormyshev VM, Tretyakov EV, Trukhin DV, Zhivetyeva SI. Trityl-based alkoxyamines as NMP controllers and spin-labels. Polymer Chemistry. 7: 6490-6499. PMID 28989533 DOI: 10.1039/C6Py01303A  0.321
2016 Audran G, Bosco L, Brémond P, Butscher T, Marque SR, Viel S. Intramolecular Hydrogen Bond Reverting the Solvent Effect on Phosphorus Hyperfine Coupling Constants of β-Phosphorylated Nitroxides. Chemphyschem : a European Journal of Chemical Physics and Physical Chemistry. 17: 3954-3963. PMID 27862794 DOI: 10.1002/Cphc.201600647  0.32
2016 Audran G, Bosco L, Nkolo P, Bikanga R, Brémond P, Butscher T, Marque SR. The β-phosphorus hyperfine coupling constant in nitroxides: 6. Solvent effects in non-cyclic nitroxides. Organic & Biomolecular Chemistry. 14: 3729-43. PMID 26986555 DOI: 10.1039/C6Ob00359A  0.312
2016 Audran G, Brémond P, Joly JP, Marque SR, Yamasaki T. C-ON bond homolysis in alkoxyamines. Part 12: the effect of the para-substituent in the 1-phenylethyl fragment. Organic & Biomolecular Chemistry. 14: 3574-83. PMID 26975717 DOI: 10.1039/C6Ob00384B  0.345
2016 Audran G, Brémond P, Marque SR, Yamasaki T. C-ON Bond Homolysis of Alkoxyamines, Part 11: Activation of the Nitroxyl Fragment. The Journal of Organic Chemistry. 81: 1981-8. PMID 26878593 DOI: 10.1021/Acs.Joc.5B02790  0.33
2016 Audran G, Bosco L, Brémond P, Butscher T, Marque SR. Solvent effect in β-phosphorylated nitroxides. Part 4: detection of traces of water by electron paramagnetic resonance. Organic & Biomolecular Chemistry. 14: 1288-92. PMID 26647997 DOI: 10.1039/C5Ob02316E  0.303
2015 Audran G, Bosco L, Brémond P, Butscher T, Franconi JM, Marque SR, Mellet P, Parzy E, Santelli M, Thiaudière E. The β-phosphorus hyperfine coupling constant in nitroxide: part 3: titration of water by electron paramagnetic resonance. Organic & Biomolecular Chemistry. 13: 11393-400. PMID 26395177 DOI: 10.1039/C5Ob01867F  0.323
2015 Audran G, Bosco L, Brémond P, Franconi JM, Koonjoo N, Marque SR, Massot P, Mellet P, Parzy E, Thiaudière E. Enzymatically Shifting Nitroxides for EPR Spectroscopy and Overhauser-Enhanced Magnetic Resonance Imaging. Angewandte Chemie (International Ed. in English). 54: 13379-84. PMID 26376730 DOI: 10.1002/Anie.201506267  0.338
2015 Audran G, Brémond P, Marque SRA, Siri D, Santelli M. Energetics of the biosynthesis of prostanes from arachidonate Tetrahedron. 71: 6920-6927. DOI: 10.1016/J.Tet.2015.07.015  0.321
2014 Audran G, Brémond P, Marque SR. Labile alkoxyamines: past, present, and future. Chemical Communications (Cambridge, England). 50: 7921-8. PMID 24817073 DOI: 10.1039/C4Cc01364F  0.33
2014 Miquet S, Brémond P, Ayela B, Marque SR, Audran G. Revised structure, total synthesis, and absolute configuration of kopeolin and kopeolone. The Journal of Organic Chemistry. 79: 2268-73. PMID 24533539 DOI: 10.1021/Jo402572B  0.315
2013 Audran G, Brémond P, Ibanou MB, Marque SR, Roubaud V, Siri D. Chemically triggered C-ON bond homolysis in alkoxyamines: regioselectivity and chemoselectivity. Organic & Biomolecular Chemistry. 11: 7738-50. PMID 24114038 DOI: 10.1039/C3Ob41549J  0.347
2013 Audran G, Brémond P, Marque SR, Obame G. Chemically triggered C-ON bond homolysis in alkoxyamines. 6. Effect of the counteranion. The Journal of Organic Chemistry. 78: 7754-7. PMID 23855482 DOI: 10.1021/Jo401227A  0.31
2013 Obame G, Brémond P, Pannecouque C, Audran G. Synthesis and Biological Evaluation of Methylenecyclopropane Analogues of Nucleosides Synthesis. 45: 2612-2618. DOI: 10.1055/S-0033-1339311  0.346
2012 Audran G, Brémond P, Marque SR, Obame G. Hyperfine coupling constants of β-phosphorylated nitroxides: a tool to probe the cybotactic effect by electron paramagnetic resonance. Chemphyschem : a European Journal of Chemical Physics and Physical Chemistry. 13: 3542-8. PMID 22887102 DOI: 10.1002/Cphc.201200420  0.304
2012 Audran G, Brémond P, Marque SRA, Obame G. Chemically triggered C–ON bond homolysis of alkoxyamines. Part 4: solvent effect Polymer Chemistry. 3: 2901-2908. DOI: 10.1039/C2Py20447A  0.323
2011 Douadi A, Brémond P, Lanez T, Pannecouque C, Audran G. Stereocontrolled Synthesis and Biological Evaluation of Novel Carbocyclic Nucleosides Analogues of Neplanocin F and Abacavir Synlett. 2011: 111-115. DOI: 10.1055/S-0030-1259100  0.322
2011 Obame G, Pellissier H, Vanthuyne N, Bongui J, Audran G. Preparation of both enantiomers of a synthon for novel nucleoside analogs by enzymatic desymmetrization of a meso-diol with a methylene cyclopropane skeleton Tetrahedron Letters. 52: 1082-1085. DOI: 10.1016/J.Tetlet.2010.12.097  0.352
2010 Candy M, Audran G, Bienaymé H, Bressy C, Pons JM. Total synthesis of (+)-crocacin C using hidden symmetry. The Journal of Organic Chemistry. 75: 1354-9. PMID 20128625 DOI: 10.1021/Jo902582W  0.354
2009 Brémond P, Vanthuyne N, Audran G. Synthesis of (+)-striatene: confirmation of its stereostructure Tetrahedron Letters. 50: 5723-5725. DOI: 10.1016/J.Tetlet.2009.07.138  0.312
2008 Brémond P, Audran G, Monti H, Clercq ED. Stereoselective Synthesis ofNovel Aristeromycin Analogues as Potential Antiviral Agents Synthesis. 2008: 3253-3260. DOI: 10.1055/S-0028-1083146  0.311
2007 Bourdron J, Commeiras L, Audran G, Vanthuyne N, Hubaud JC, Parrain JL. First total synthesis and assignment of the stereochemistry of crispatenine. The Journal of Organic Chemistry. 72: 3770-5. PMID 17441771 DOI: 10.1021/Jo070045J  0.332
2007 Brémond P, Audran G, Aubin Y, Monti H. Total Chemoenzymatic Synthesis of (-)-3′-Methylaristeromycin Synlett. 2007: 1124-1126. DOI: 10.1055/S-2007-973889  0.349
2006 Aubin Y, Audran G, Monti H. Conformationally locked carbocyclic nucleosides : Synthesis of the 1-methyl- 6-oxabicyclo[3.1.0]hexane scaffold Synlett. 2006: 2215-2218. DOI: 10.1055/S-2006-949635  0.326
2006 Palombo E, Audran G, Monti H. Enantioconvergent access to the enantiomerically pure building blocks (+)- or (-)-4-hydroxy-3-methyl-2-cyclohexenone using a chemoenzymatic process Synlett. 2006: 403-406. DOI: 10.1055/S-2006-926258  0.326
2006 Aubin Y, Audran G, Monti H. Improved enantioselective synthesis of natural striatenic acid and its methyl ester Tetrahedron Letters. 47: 3669-3671. DOI: 10.1016/J.Tetlet.2006.03.147  0.311
2005 Palombo E, Audran G, Monti H. Enantioselective Synthesis of (+)-Ricciocarpin A Using an Auxiliary Hydroxyl Group and a Diastereofacial Selectivity Based Methodology Synlett. 2005: 2104-2106. DOI: 10.1055/S-2005-871932  0.333
2004 Acherar S, Audran G, Cecchin F, Monti H. Enantioselective synthesis of natural (−)-tochuinyl acetate, (−)-dihydrotochuinyl acetate and (+)-β-cuparenone using both enantiomers of the same building block Tetrahedron. 60: 5907-5912. DOI: 10.1016/J.Tet.2004.05.037  0.328
2003 Uttaro JP, Audran G, Palombo E, Monti H. First enantioselective synthesis and absolute stereochemistry assignment of new monocyclic sesquiterpenes from Artemisia chamaemelifolia. The Journal of Organic Chemistry. 68: 5407-10. PMID 12816510 DOI: 10.1021/Jo034424Y  0.313
2003 Palombo E, Audran G, Monti H. First enantioselective synthesis and determination of the absolute configuration of natural (+)-dehydro-β-monocyclonerolidol Tetrahedron Letters. 44: 6463-6464. DOI: 10.1016/S0040-4039(03)01562-4  0.312
2002 Audran G, Uttaro J, Monti H. Enantioselective taxanes approach using both enantiomers of the same building-block. Part 1: Taxol® a-ring subunit Synlett. 2002: 1261-1264. DOI: 10.1055/S-2002-32968  0.313
2001 Galano JM, Audran G, Monti H. First enantioselective total synthesis of both enantiomers of lancifolol. Correlation: Absolute configuration/specific rotation Tetrahedron Letters. 42: 6125-6128. DOI: 10.1016/S0040-4039(01)01202-3  0.318
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