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Eric Defrancq - Publications

Affiliations: 
Université Grenoble Alpes, France 
Area:
Synthetic Organic Chemistry, syntheses and modifications of oligonucleotides
Website:
https://dcm.univ-grenoble-alpes.fr/membre/eric-defrancq
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36 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 Devaux A, Bonnat L, Lavergne T, Defrancq E. Access to a stabilized i-motif DNA structure through four successive ligation reactions on a cyclopeptide scaffold. Organic & Biomolecular Chemistry. PMID 32756719 DOI: 10.1039/D0Ob01311K  0.342
2015 Estalayo-Adriàn S, Lartia R, Meyer A, Vasseur JJ, Morvan F, Defrancq E. Assessment of the Full Compatibility of Copper(I)-Catalyzed Alkyne-Azide Cycloaddition and Oxime Click Reactions for bis-Labelling of Oligonucleotides. Chemistryopen. 4: 169-73. PMID 25969815 DOI: 10.1002/open.201402099  0.328
2013 Moreau J, Dendane N, Schöllhorn B, Spinelli N, Fave C, Defrancq E. Synthesis and characterization of oligonucleotide conjugates bearing electroactive labels. Bioorganic & Medicinal Chemistry Letters. 23: 955-8. PMID 23324407 DOI: 10.1016/j.bmcl.2012.12.057  0.333
2013 Spinelli N, Defrancq E, Morvan F. Glycoclusters on oligonucleotide and PNA scaffolds: synthesis and applications. Chemical Society Reviews. 42: 4557-73. PMID 23254681 DOI: 10.1039/c2cs35406c  0.361
2012 Lartia R, Bonnat L, Murat P, Defrancq E. Preparation of azido containing oligonucleotides through diazo transfer reaction. Current Protocols in Nucleic Acid Chemistry / Edited by Serge L. Beaucage ... [Et Al.]. Unit4.50. PMID 22956456 DOI: 10.1002/0471142700.Nc0450S50  0.309
2012 Bonnet R, Murat P, Spinelli N, Defrancq E. Click-click chemistry on a peptidic scaffold for easy access to tetrameric DNA structures. Chemical Communications (Cambridge, England). PMID 22576321 DOI: 10.1039/C2Cc32010J  0.327
2011 Murat P, Singh Y, Defrancq E. Methods for investigating G-quadruplex DNA/ligand interactions. Chemical Society Reviews. 40: 5293-307. PMID 21720638 DOI: 10.1039/C1Cs15117G  0.59
2010 Singh Y, Murat P, Defrancq E. Recent developments in oligonucleotide conjugation. Chemical Society Reviews. 39: 2054-70. PMID 20393645 DOI: 10.1039/B911431A  0.643
2010 Foret D, Renaudet O, Boturyn D, Defrancq E, Dumy P. ChemInform Abstract: 3′-Oligonucleotides Conjugation via Chemoselective Oxime Bond Formation. Cheminform. 33: no-no. DOI: 10.1002/CHIN.200210205  0.338
2010 Forget D, Boturyn D, Defrancq E, Lhomme J, Dumy P. ChemInform Abstract: Highly Efficient Synthesis of Peptide - Oligonucleotide Conjugates: Chemoselective Oxime and Thiazolidine Formation. Cheminform. 33: no-no. DOI: 10.1002/CHIN.200206255  0.372
2010 Forget D, Renaudet O, Defrancq E, Dumy P. ChemInform Abstract: Efficient Preparation of Carbohydrate-Oligonucleotide Conjugates (COCs) Using Oxime Bond Formation. Cheminform. 33: no-no. DOI: 10.1002/CHIN.200203220  0.38
2009 Murat P, Spinelli N, Dumy P, Defrancq E. Efficient conjugation of oligonucleotides through aromatic oxime formation. Bioorganic & Medicinal Chemistry Letters. 19: 6534-7. PMID 19857965 DOI: 10.1016/J.Bmcl.2009.10.048  0.383
2008 Murat P, Cressend D, Spinelli N, Van der Heyden A, Labbé P, Dumy P, Defrancq E. A novel conformationally constrained parallel g quadruplex. Chembiochem : a European Journal of Chemical Biology. 9: 2588-91. PMID 18821555 DOI: 10.1002/Cbic.200800457  0.32
2008 Spinelli N, Singh Y, Defrancq E, Dumy P. Aldehydic oligonucleotide: a key intermediate for the preparation of oligonucleotide conjugates through oxime bond formation. Nucleosides, Nucleotides & Nucleic Acids. 26: 883-7. PMID 18058501 DOI: 10.1080/15257770701505436  0.677
2008 Defrancq E, Singh Y, Spinelli N. Chemical Strategies for Oligonucleotide-Conjugates Synthesis Current Organic Chemistry. 12: 263-290. DOI: 10.2174/138527208783743732  0.655
2008 Singh Y, Spinelli N, Defrancq E. ChemInform Abstract: Chemical Strategies for Oligonucleotide-Conjugate Synthesis Cheminform. 39. DOI: 10.1002/CHIN.200842236  0.654
2008 Villien M, Deroo S, Gicquel E, Defrancq E, Moucheron C, Kirsch-De Mesmaeker A, Dumy P. ChemInform Abstract: The Oxime Bond Formation as an Efficient Tool for the Conjugation of Ruthenium Complexes to Oligonucleotides and Peptides. Cheminform. 39. DOI: 10.1002/CHIN.200807178  0.355
2007 Spinelli N, Edupuganti OP, Defrancq E, Dumy P. New solid support for the synthesis of 3'-oligonucleotide conjugates through glyoxylic oxime bond formation. Organic Letters. 9: 219-22. PMID 17217269 DOI: 10.1021/ol062607b  0.445
2007 Villien M, Deroo S, Gicquel E, Defrancq E, Moucheron C, Kirsch-De Mesmaeker A, Dumy P. The oxime bond formation as an efficient tool for the conjugation of ruthenium complexes to oligonucleotides and peptides Tetrahedron. 63: 11299-11306. DOI: 10.1016/J.TET.2007.08.088  0.345
2006 Singh Y, Spinelli N, Defrancq E, Dumy P. A novel heterobifunctional linker for facile access to bioconjugates. Organic & Biomolecular Chemistry. 4: 1413-9. PMID 16557331 DOI: 10.1039/b518151h  0.659
2006 Garanger E, Boturyn D, Renaudet O, Defrancq E, Dumy P. Chemoselectively addressable template: a valuable tool for the engineering of molecular conjugates. The Journal of Organic Chemistry. 71: 2402-10. PMID 16526790 DOI: 10.1021/Jo0525480  0.35
2006 Singh Y, Edupuganti OP, Villien M, Defrancq E, Dumy P. The Oxime Bond Formation as a Useful Tool for the Preparation of Oligonucleotide Conjugates Cheminform. 37. DOI: 10.1002/CHIN.200616249  0.644
2005 Singh Y, Renaudet O, Defrancq E, Dumy P. Preparation of a multitopic glycopeptide-oligonucleotide conjugate. Organic Letters. 7: 1359-62. PMID 15787506 DOI: 10.1021/Ol050134N  0.637
2005 Singh Y, Edupuganti OP, Villien M, Defrancq É, Dumy P. The oxime bond formation as a useful tool for the preparation of oligonucleotide conjugates Comptes Rendus Chimie. 8: 789-796. DOI: 10.1016/J.CRCI.2005.02.007  0.644
2004 Villien M, Defrancq E, Dumy P. Chemoselective oxime and thiazolidine bond formation: a versatile and efficient route to the preparation of 3'-peptide-oligonucleotide conjugates. Nucleosides, Nucleotides & Nucleic Acids. 23: 1657-66. PMID 15620102 DOI: 10.1081/NCN-200031467  0.41
2004 Singh Y, Defrancq E, Dumy P. New method to prepare peptide-oligonucleotide conjugates through glyoxylic oxime formation. The Journal of Organic Chemistry. 69: 8544-6. PMID 15549841 DOI: 10.1021/jo0485177  0.662
2004 Edupuganti OP, Singh Y, Defrancq E, Dumy P. New strategy for the synthesis of 3',5'-bifunctionalized oligonucleotide conjugates through sequential formation of chemoselective oxime bonds. Chemistry (Weinheim An Der Bergstrasse, Germany). 10: 5988-95. PMID 15497169 DOI: 10.1002/chem.200400390  0.665
2004 Ghosh S, Defrancq E, Lhomme JH, Dumy P, Bhattacharya S. Efficient conjugation and characterization of distamycin-based peptides with selected oligonucleotide stretches. Bioconjugate Chemistry. 15: 520-529. PMID 15149179 DOI: 10.1021/Bc0341730  0.464
2004 Edupuganti OP, Renaudet O, Defrancq E, Dumy P. The oxime bond formation as an efficient chemical tool for the preparation of 3',5'-bifunctionalised oligodeoxyribonucleotides. Bioorganic & Medicinal Chemistry Letters. 14: 2839-42. PMID 15125943 DOI: 10.1016/J.Bmcl.2004.03.053  0.448
2004 Forget D, Boturyn D, Renaudet O, Defrancq E, Dumy P. Highly Efficient Synthesis of Peptide- and Carbohydrate-Oligonucleotide Conjugates Using Chemoselective Oxime and Thiazolidine Formation Cheminform. 35. DOI: 10.1002/CHIN.200407263  0.365
2003 Edupuganti OP, Defrancq E, Dumy P. Head-to-tail oxime cyclization of oligodeoxynucleotides for the efficient synthesis of circular DNA analogues. The Journal of Organic Chemistry. 68: 8708-10. PMID 14575507 DOI: 10.1021/jo035064h  0.435
2003 Forget D, Boturyn D, Renaudet O, Defrancq E, Dumy P. Highly efficient synthesis of peptide- and carbohydrate-oligonucleotide conjugates using chemoselective oxime and thiazolidine formation. Nucleosides, Nucleotides & Nucleic Acids. 22: 1427-9. PMID 14565434 DOI: 10.1081/Ncn-120023001  0.365
2003 Deroo S, Defrancq E, Moucheron C, Kirsch-De Mesmaeker A, Dumy P. Synthesis of an oxyamino-containing phenanthroline derivative for the efficient preparation of phenanthroline oligonucleotide oxime conjugates Tetrahedron Letters. 44: 8379-8382. DOI: 10.1016/J.TETLET.2003.09.128  0.355
2001 Forget D, Boturyn D, Defrancq E, Lhomme J, Dumy P. Highly efficient synthesis of peptide-oligonucleotide conjugates: chemoselective oxime and thiazolidine formation. Chemistry (Weinheim An Der Bergstrasse, Germany). 7: 3976-84. PMID 11596939 DOI: 10.1002/1521-3765(20010917)7:18<3976::AID-CHEM3976>3.0.CO;2-X  0.404
2001 Forget D, Renaudet O, Boturyn D, Defrancq E, Dumy P. 3′-Oligonucleotides conjugation via chemoselective oxime bond formation Tetrahedron Letters. 42: 9171-9174. DOI: 10.1016/S0040-4039(01)02017-2  0.418
2001 Forget D, Renaudet O, Defrancq E, Dumy P. Efficient preparation of carbohydrate–oligonucleotide conjugates (COCs) using oxime bond formation Tetrahedron Letters. 42: 7829-7832. DOI: 10.1016/S0040-4039(01)01682-3  0.423
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