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Page 1
Asymmetric Strecker synthesis of α-arylglycines.
Pérez-Fuertes Y, Taylor JE, Tickell DA, Mahon MF, Bull SD, James TD. Pérez-Fuertes Y, et al. J Org Chem. 2011 Aug 5;76(15):6038-47. doi: 10.1021/jo200528s. Epub 2011 Jun 27. J Org Chem. 2011. PMID: 21627154
The stereochemical course of bromoetherification of enynes.
Christopher Braddock D, Bhuva R, Pérez-Fuertes Y, Pouwer R, Roberts CA, Ruggiero A, Stokes ES, White AJ. Christopher Braddock D, et al. Among authors: perez fuertes y. Chem Commun (Camb). 2008 Mar 28;(12):1419-21. doi: 10.1039/b800054a. Epub 2008 Feb 20. Chem Commun (Camb). 2008. PMID: 18338042
Design, synthesis and structure-activity relationships of a novel class of sulfonylpyridine inhibitors of Interleukin-2 inducible T-cell kinase (ITK).
Trani G, Barker JJ, Bromidge SM, Brookfield FA, Burch JD, Chen Y, Eigenbrot C, Heifetz A, Ismaili MHA, Johnson A, Krülle TM, MacKinnon CH, Maghames R, McEwan PA, Montalbetti CAGN, Ortwine DF, Pérez-Fuertes Y, Vaidya DG, Wang X, Zarrin AA, Pei Z. Trani G, et al. Among authors: perez fuertes y. Bioorg Med Chem Lett. 2014 Dec 15;24(24):5818-5823. doi: 10.1016/j.bmcl.2014.10.020. Epub 2014 Oct 12. Bioorg Med Chem Lett. 2014. PMID: 25455497
7-(Pyrazol-4-yl)-3H-imidazo[4,5-b]pyridine-based derivatives for kinase inhibition: Co-crystallisation studies with Aurora-A reveal distinct differences in the orientation of the pyrazole N1-substituent.
Bavetsias V, Pérez-Fuertes Y, McIntyre PJ, Atrash B, Kosmopoulou M, O'Fee L, Burke R, Sun C, Faisal A, Bush K, Avery S, Henley A, Raynaud FI, Linardopoulos S, Bayliss R, Blagg J. Bavetsias V, et al. Among authors: perez fuertes y. Bioorg Med Chem Lett. 2015 Oct 1;25(19):4203-9. doi: 10.1016/j.bmcl.2015.08.003. Epub 2015 Aug 6. Bioorg Med Chem Lett. 2015. PMID: 26296477 Free PMC article.
12 results