García-Tellado F - Search Results

1

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. Org Lett. 2001 Jun 14;3(12):1905-8. doi: 10.1021/ol015951b. Org Lett. 2001. PMID: 11405741

2

Highly 1,2-trans Stereoselective Allylations of 1,2-O-Isopropylidene-Protected Glycofuranosides This work was supported by the Canary Islands Consejería de Educación y Ciencia (PI1998/109), the Spanish Comisión Interministerial de Ciencia y Tecnología (PB98-0443-C02-02), and the FEDER (1SD97-0747-C04-01).

García-Tellado F, de Armas P, Marrero-Tellado JJ. García-Tellado F, et al. Angew Chem Int Ed Engl. 2000 Aug 4;39(15):2727-2729. doi: 10.1002/1521-3773(20000804)39:15<2727::aid-anie2727>3.0.co;2-i. Angew Chem Int Ed Engl. 2000. PMID: 10934407 No abstract available.

3

Highly 2,3-trans stereoselective allylations of 2, 3-O-isopropylidene-protected pyrrolidines: circumventing the N-acyliminium ion chemistry?

de Armas P, García-Tellado F, Marrero-Tellado JJ. de Armas P, et al. Org Lett. 2000 Nov 2;2(22):3513-5. doi: 10.1021/ol006574q. Org Lett. 2000. PMID: 11082022

4

An effective one-pot synthesis of 5-substituted tetronic acids.

Aragón DT, López GV, García-Tellado F, Marrero-Tellado JJ, de Armas P, Terrero D. Aragón DT, et al. J Org Chem. 2003 Apr 18;68(8):3363-5. doi: 10.1021/jo034083o. J Org Chem. 2003. PMID: 12688823 Free article.

5

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

6

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.

7

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.

8

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

9

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. 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

10

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

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