Tejedor D - Search Results

1

A green multicomponent synthesis of tocopherol analogues with antiproliferative activities.

Ingold M, Dapueto R, Victoria S, Galliusi G, Batthyàny C, Bollati-Fogolín M, Tejedor D, García-Tellado F, Padrón JM, Porcal W, López GV. Ingold M, et al. Among authors: tejedor d. Eur J Med Chem. 2018 Jan 1;143:1888-1902. doi: 10.1016/j.ejmech.2017.11.003. Epub 2017 Nov 3. Eur J Med Chem. 2018. PMID: 29129514

2

Alkynoates as a source of reactive alkylinides for aldehyde addition reactions.

de Armas P, García-Tellado F, Marrero-Tellado JJ, Tejedor D, Maestro MA, Gonzalez-Platas J. de Armas P, et al. Among authors: tejedor d. Org Lett. 2001 Jun 14;3(12):1905-8. doi: 10.1021/ol015951b. Org Lett. 2001. PMID: 11405741

3

Efficient domino process based on the catalytic generation of non-metalated, conjugated acetylides in the presence of aldehydes or activated ketones.

Tejedor D, García-Tellado F, Marrero-Tellado JJ, de Armas P. Tejedor D, et al. Chemistry. 2003 Jul 7;9(13):3122-31. doi: 10.1002/chem.200204579. Chemistry. 2003. PMID: 12833294

4

A diversity-oriented strategy for the construction of tetrasubstituted pyrroles via coupled domino processes.

Tejedor D, González-Cruz D, García-Tellado F, Marrero-Tellado JJ, Rodríguez ML. Tejedor D, et al. J Am Chem Soc. 2004 Jul 14;126(27):8390-1. doi: 10.1021/ja047396p. J Am Chem Soc. 2004. PMID: 15237991 Free article.

5

A modular, one-pot, four-component synthesis of polysubstituted 1,3-oxazolidines.

Tejedor D, Santos-Expósito A, González-Cruz D, Marrero-Tellado JJ, García-Tellado F. Tejedor D, et al. J Org Chem. 2005 Feb 4;70(3):1042-5. doi: 10.1021/jo048469q. J Org Chem. 2005. PMID: 15675866 Free article.

6

Multicomponent domino processes based on the organocatalytic generation of conjugated acetylides: efficient synthetic manifolds for diversity-oriented molecular construction.

Tejedor D, González-Cruz D, Santos-Expósito A, Marrero-Tellado JJ, de Armas P, García-Tellado F. Tejedor D, et al. Chemistry. 2005 Jun 6;11(12):3502-10. doi: 10.1002/chem.200401267. Chemistry. 2005. PMID: 15754384

7

Antiproliferative activity in HL60 cells by tetrasubstituted pyrroles: a structure-activity relationship study.

Padrón JM, Tejedor D, Santos-Expósito A, García-Tellado F, Martín VS, Villar J. Padrón JM, et al. Among authors: tejedor d. Bioorg Med Chem Lett. 2005 May 16;15(10):2487-90. doi: 10.1016/j.bmcl.2005.03.069. Bioorg Med Chem Lett. 2005. PMID: 15863302

8

Chemo-differentiating MCRs based on alpha-ketoesters and terminal alkynoates. A homoaldol-based ABB' system.

Tejedor D, Santos-Expósito A, García-Tellado F. Tejedor D, et al. Chem Commun (Camb). 2006 Jul 5;(25):2667-9. doi: 10.1039/b605075a. Epub 2006 May 18. Chem Commun (Camb). 2006. PMID: 16786081

9

Organocatalysis "on water". Regioselective [3 + 2]-cycloaddition of nitrones and allenolates.

González-Cruz D, Tejedor D, de Armas P, Morales EQ, García-Tellado F. González-Cruz D, et al. Among authors: tejedor d. Chem Commun (Camb). 2006 Jul 14;(26):2798-800. doi: 10.1039/b606096j. Chem Commun (Camb). 2006. PMID: 17009467

10

A substrate-based folding process incorporating chemodifferentiating ABB' three-component reactions of terminal alkynoates and 1,2-dicarbonyl compounds: a skeletal-diversity-oriented synthetic manifold.

Tejedor D, Sántos-Expósito A, García-Tellado F. Tejedor D, et al. Chemistry. 2007;13(4):1201-9. doi: 10.1002/chem.200600749. Chemistry. 2007. PMID: 17075926

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