Falomir E - Search Results

1

Aryl Urea Based Scaffolds for Multitarget Drug Discovery in Anticancer Immunotherapies.

Martín-Beltrán C, Gil-Edo R, Hernández-Ribelles G, Agut R, Marí-Mezquita P, Carda M, Falomir E. Martín-Beltrán C, et al. Among authors: falomir e. Pharmaceuticals (Basel). 2021 Apr 6;14(4):337. doi: 10.3390/ph14040337. Pharmaceuticals (Basel). 2021. PMID: 33917617 Free PMC article.

2

Chlorodicyclohexylborane-mediated aldol additions of alpha,alpha'-dioxygenated ketones.

Murga J, Falomir E, Carda M, González F, Marco JA. Murga J, et al. Among authors: falomir e. Org Lett. 2001 Mar 22;3(6):901-4. doi: 10.1021/ol015542f. Org Lett. 2001. PMID: 11263911

3

Stereoselective synthesis of microcarpalide.

Murga J, Falomir E, García-Fortanet J, Carda M, Marco JA. Murga J, et al. Among authors: falomir e. Org Lett. 2002 Oct 3;4(20):3447-9. doi: 10.1021/ol0265463. Org Lett. 2002. PMID: 12323040

4

Stereoselective synthesis and determination of the cytotoxic properties of spicigerolide and three of its stereoisomers.

Falomir E, Murga J, Ruiz P, Carda M, Marco JA, Pereda-Miranda R, Fragoso-Serrano M, Cerda-García-Rojas CM. Falomir E, et al. J Org Chem. 2003 Jul 11;68(14):5672-6. doi: 10.1021/jo034470y. J Org Chem. 2003. PMID: 12839461

5

Double diastereoselection in aldol reactions mediated by dicyclohexylchloroborane between L-erythrulose derivatives and chiral aldehydes. The Felkin-Anh versus Cornforth dichotomy.

Marco JA, Carda M, Díaz-Oltra S, Murga J, Falomir E, Roeper H. Marco JA, et al. Among authors: falomir e. J Org Chem. 2003 Oct 31;68(22):8577-82. doi: 10.1021/jo035159j. J Org Chem. 2003. PMID: 14575488

6

Stereoselective anti aldol reactions of erythrulose derivatives. Functionalized chiral d3 and d4 synthons.

Murga J, Ruiz P, Falomir E, Carda M, Peris G, Marco JA. Murga J, et al. Among authors: falomir e. J Org Chem. 2004 Mar 19;69(6):1987-92. doi: 10.1021/jo0356356. J Org Chem. 2004. PMID: 15058944

7

Double diastereoselection in aldol reactions mediated by dicyclohexylchloroborane between chiral aldehydes and a chiral ethyl ketone derived from L-erythrulose. synthesis of a C1-C9 fragment of the structure of the antifungal metabolite soraphen A1alpha.

Díaz-Oltra S, Murga J, Falomir E, Carda M, Peris G, Marco JA. Díaz-Oltra S, et al. Among authors: falomir e. J Org Chem. 2005 Sep 30;70(20):8130-9. doi: 10.1021/jo051307p. J Org Chem. 2005. PMID: 16277339

8

Stereoselective total synthesis and absolute configuration of the natural decanolides (-)-microcarpalide and (+)-lethaloxin. Identity of (+)-lethaloxin and (+)-pinolidoxin.

García-Fortanet J, Murga J, Falomir E, Carda M, Marco JA. García-Fortanet J, et al. Among authors: falomir e. J Org Chem. 2005 Nov 25;70(24):9822-7. doi: 10.1021/jo051353p. J Org Chem. 2005. PMID: 16292811

9

Stereoselective synthesis of the glycosidase inhibitor australine through a one-pot, double-cyclization strategy.

Ribes C, Falomir E, Carda M, Marco JA. Ribes C, et al. Among authors: falomir e. Org Lett. 2007 Jan 4;9(1):77-80. doi: 10.1021/ol062570v. Org Lett. 2007. PMID: 17192089

10

Aldol reactions between L-erythrulose derivatives and chiral alpha-amino and alpha-fluoro aldehydes: competition between Felkin-Anh and Cornforth transition states.

Díaz-Oltra S, Carda M, Murga J, Falomir E, Marco JA. Díaz-Oltra S, et al. Among authors: falomir e. Chemistry. 2008;14(30):9240-54. doi: 10.1002/chem.200800956. Chemistry. 2008. PMID: 18756569

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