Behr JB - Search Results

1

Synthesis and fucosidase inhibitory study of unnatural pyrrolidine alkaloid 4-epi-(+)-codonopsinine.

Kotland A, Accadbled F, Robeyns K, Behr JB. Kotland A, et al. Among authors: behr jb. J Org Chem. 2011 May 20;76(10):4094-8. doi: 10.1021/jo200176u. Epub 2011 Apr 28. J Org Chem. 2011. PMID: 21495694

2

Spirocyclopropyl pyrrolidines as a new series of alpha-L-fucosidase inhibitors.

Laroche C, Behr JB, Szymoniak J, Bertus P, Schütz C, Vogel P, Plantier-Royon R. Laroche C, et al. Among authors: behr jb. Bioorg Med Chem. 2006 Jun 15;14(12):4047-54. doi: 10.1016/j.bmc.2006.02.005. Epub 2006 Feb 20. Bioorg Med Chem. 2006. PMID: 16488612

3

Tandem nucleophilic addition/cyclization reaction in the synthesis of ketimine-type iminosugars.

Behr JB, Kalla A, Harakat D, Plantier-Royon R. Behr JB, et al. J Org Chem. 2008 May 2;73(9):3612-5. doi: 10.1021/jo702616x. Epub 2008 Mar 22. J Org Chem. 2008. PMID: 18357997

4

The spirocyclopropyl moiety as a methyl surrogate in the structure of l-fucosidase and l-rhamnosidase inhibitors.

Pearson MS, Floquet N, Bello C, Vogel P, Plantier-Royon R, Szymoniak J, Bertus P, Behr JB. Pearson MS, et al. Among authors: behr jb. Bioorg Med Chem. 2009 Dec 1;17(23):8020-6. doi: 10.1016/j.bmc.2009.10.010. Epub 2009 Oct 12. Bioorg Med Chem. 2009. PMID: 19875298

5

Synthesis and glycosidase inhibitory activity of 1-amino-3,6-anhydro-1-deoxy-D-sorbitol derivatives.

Guillarme S, Behr JB, Bello C, Vogel P, Saluzzo C. Guillarme S, et al. Among authors: behr jb. Bioorg Chem. 2010 Apr;38(2):43-7. doi: 10.1016/j.bioorg.2009.12.002. Epub 2009 Dec 5. Bioorg Chem. 2010. PMID: 20060997

6

Iminosugar-ferrocene conjugates as potential anticancer agents.

Hottin A, Dubar F, Steenackers A, Delannoy P, Biot C, Behr JB. Hottin A, et al. Among authors: behr jb. Org Biomol Chem. 2012 Aug 7;10(29):5592-7. doi: 10.1039/c2ob25727k. Epub 2012 Jun 20. Org Biomol Chem. 2012. PMID: 22717621

7

α-L-fucosidase inhibition by pyrrolidine-ferrocene hybrids: rationalization of ligand-binding properties by structural studies.

Hottin A, Wright DW, Steenackers A, Delannoy P, Dubar F, Biot C, Davies GJ, Behr JB. Hottin A, et al. Among authors: behr jb. Chemistry. 2013 Jul 15;19(29):9526-33. doi: 10.1002/chem.201301001. Epub 2013 Jun 5. Chemistry. 2013. PMID: 23740878

8

Trifluoromethide as a strong base: [CF3-] mediates dichloromethylation of nitrones by proton abstraction from the solvent.

Behr JB, Chavaria D, Plantier-Royon R. Behr JB, et al. J Org Chem. 2013 Nov 15;78(22):11477-82. doi: 10.1021/jo402028r. Epub 2013 Oct 24. J Org Chem. 2013. PMID: 24111552

9

Exploiting the hydrophobic terrain in fucosidases with aryl-substituted pyrrolidine iminosugars.

Hottin A, Wright DW, Davies GJ, Behr JB. Hottin A, et al. Among authors: behr jb. Chembiochem. 2015 Jan 19;16(2):277-83. doi: 10.1002/cbic.201402509. Epub 2014 Nov 26. Chembiochem. 2015. PMID: 25427942

10

Synthesis of 2-carboxymethyl polyhydroxyazepanes and their evaluation as glycosidase inhibitors.

Taghzouti H, Goumain S, Harakat D, Portella C, Behr JB, Plantier-Royon R. Taghzouti H, et al. Among authors: behr jb. Bioorg Chem. 2015 Feb;58:11-7. doi: 10.1016/j.bioorg.2014.11.003. Epub 2014 Nov 13. Bioorg Chem. 2015. PMID: 25462622

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