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Page 1
Catalytic oxyamidation of indoles.
Beaumont S, Pons V, Retailleau P, Dodd RH, Dauban P. Beaumont S, et al. Among authors: dodd rh. Angew Chem Int Ed Engl. 2010 Feb 22;49(9):1634-7. doi: 10.1002/anie.200906650. Angew Chem Int Ed Engl. 2010. PMID: 20112323 No abstract available.
Azetidinimines as a novel series of non-covalent broad-spectrum inhibitors of β-lactamases with submicromolar activities against carbapenemases KPC-2 (class A), NDM-1 (class B) and OXA-48 (class D).
Romero E, Oueslati S, Benchekroun M, D'Hollander ACA, Ventre S, Vijayakumar K, Minard C, Exilie C, Tlili L, Retailleau P, Zavala A, Elisée E, Selwa E, Nguyen LA, Pruvost A, Naas T, Iorga BI, Dodd RH, Cariou K. Romero E, et al. Among authors: dodd rh. Eur J Med Chem. 2021 Jul 5;219:113418. doi: 10.1016/j.ejmech.2021.113418. Epub 2021 Apr 2. Eur J Med Chem. 2021. PMID: 33862516
Synthesis and benzodiazepine receptor affinities of rigid analogues of 3-carboxy-beta-carbolines: demonstration that the benzodiazepine receptor recognizes preferentially the s-cis conformation of the 3-carboxy group.
Dorey G, Poissonnet G, Potier MC, Prado de Carvalho L, Venault P, Chapouthier G, Rossier J, Potier P, Dodd RH. Dorey G, et al. Among authors: dodd rh. J Med Chem. 1989 Aug;32(8):1799-804. doi: 10.1021/jm00128a023. J Med Chem. 1989. PMID: 2547070
Synthesis of 6-hydroxyaurone analogues and evaluation of their α-glucosidase inhibitory and glucose consumption-promoting activity: Development of highly active 5,6-disubstituted derivatives.
Sun H, Ding W, Song X, Wang D, Chen M, Wang K, Zhang Y, Yuan P, Ma Y, Wang R, Dodd RH, Zhang Y, Lu K, Yu P. Sun H, et al. Among authors: dodd rh. Bioorg Med Chem Lett. 2017 Aug 1;27(15):3226-3230. doi: 10.1016/j.bmcl.2017.06.040. Epub 2017 Jun 15. Bioorg Med Chem Lett. 2017. PMID: 28651984
185 results