Dumy P - Search Results

1

Expanding the scope of oxime ligation: facile synthesis of large cyclopeptide-based glycodendrimers.

Thomas B, Berthet N, Garcia J, Dumy P, Renaudet O. Thomas B, et al. Among authors: dumy p. Chem Commun (Camb). 2013 Nov 28;49(92):10796-8. doi: 10.1039/c3cc45368e. Chem Commun (Camb). 2013. PMID: 24121458

2

Methyl 2,3,6-tri-O-benzoyl-4-deoxy-4-methoxyamino-alpha-D-glucopyranoside.

Renaudet O, Dumy P, Philouze C. Renaudet O, et al. Among authors: dumy p. Acta Crystallogr C. 2001 Mar;57(Pt 3):309-10. doi: 10.1107/s0108270100019387. Acta Crystallogr C. 2001. PMID: 11250589

3

N-(2-Acetamido-3,4,6-tri-O-acetyl-2-deoxy-alpha-D-galactopyranosyloxy)succinimide.

Renaudet O, Dumy P, Philouze C, Averbuch-Pouchot MT. Renaudet O, et al. Among authors: dumy p. Acta Crystallogr C. 2001 May;57(Pt 5):649-50. doi: 10.1107/s0108270101003377. Epub 2001 May 15. Acta Crystallogr C. 2001. PMID: 11353281

4

Highly efficient synthesis of peptide-oligonucleotide conjugates: chemoselective oxime and thiazolidine formation.

Forget D, Boturyn D, Defrancq E, Lhomme J, Dumy P. Forget D, et al. Among authors: dumy p. Chemistry. 2001 Sep 17;7(18):3976-84. doi: 10.1002/1521-3765(20010917)7:18<3976::aid-chem3976>3.0.co;2-x. Chemistry. 2001. PMID: 11596939

5

Chemoselectively template-assembled glycoconjugates as mimics for multivalent presentation of carbohydrates.

Renaudet O, Dumy P. Renaudet O, et al. Among authors: dumy p. Org Lett. 2003 Feb 6;5(3):243-6. doi: 10.1021/ol0270935. Org Lett. 2003. PMID: 12556162

6

Highly efficient synthesis of peptide- and carbohydrate-oligonucleotide conjugates using chemoselective oxime and thiazolidine formation.

Forget D, Boturyn D, Renaudet O, Defrancq E, Dumy P. Forget D, et al. Among authors: dumy p. Nucleosides Nucleotides Nucleic Acids. 2003 May-Aug;22(5-8):1427-9. doi: 10.1081/NCN-120023001. Nucleosides Nucleotides Nucleic Acids. 2003. PMID: 14565434 No abstract available.

7

Head-to-tail oxime cyclization of oligodeoxynucleotides for the efficient synthesis of circular DNA analogues.

Edupuganti OP, Defrancq E, Dumy P. Edupuganti OP, et al. Among authors: dumy p. J Org Chem. 2003 Oct 31;68(22):8708-10. doi: 10.1021/jo035064h. J Org Chem. 2003. PMID: 14575507

8

The oxime bond formation as an efficient chemical tool for the preparation of 3',5'-bifunctionalised oligodeoxyribonucleotides.

Edupuganti OP, Renaudet O, Defrancq E, Dumy P. Edupuganti OP, et al. Among authors: dumy p. Bioorg Med Chem Lett. 2004 Jun 7;14(11):2839-42. doi: 10.1016/j.bmcl.2004.03.053. Bioorg Med Chem Lett. 2004. PMID: 15125943

9

New strategy for the synthesis of 3',5'-bifunctionalized oligonucleotide conjugates through sequential formation of chemoselective oxime bonds.

Edupuganti OP, Singh Y, Defrancq E, Dumy P. Edupuganti OP, et al. Among authors: dumy p. Chemistry. 2004 Nov 19;10(23):5988-95. doi: 10.1002/chem.200400390. Chemistry. 2004. PMID: 15497169

10

New method to prepare peptide-oligonucleotide conjugates through glyoxylic oxime formation.

Singh Y, Defrancq E, Dumy P. Singh Y, et al. Among authors: dumy p. J Org Chem. 2004 Nov 26;69(24):8544-6. doi: 10.1021/jo0485177. J Org Chem. 2004. PMID: 15549841

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