Grupo de Síntesis Orgánica

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Publicaciones desde el año 2000

  1. Design and synthesis of pironetin analogues with simplified structure and study of their interactions with microtubules. J. A. Marco, J. García-Pla, M. Carda, J. Murga, Eva Falomir, C. Trigili, S. Notararigo, J. F. Díaz, I. Barasoain. Eur. J. Med. Chem. 2011, 46, 1630-1637.

  2. Stereoselective Synthesis of Five Biologically Active, Naturally Occurring Medium and Large Ring Lactones. J. A. Marco, M. Carda. Nat. Prod. Commun. 2011, 6, 505-514.

  3. Synthesis and Biological Properties of the Cytotoxic 14-Membered Macrolides Aspergillide A and B. S. Díaz-Oltra, C. A. Angulo-Pachón, J. Murga, E. Falomir, M. Carda, J. A. Marco. Chem. Eur. J. 2011, 17, 675-688.

  4. Stereoselective Synthesis and Structural Correction of the Naturally Occurring Lactone Stagonolide G. C. A. Angulo-Pachón, S. Díaz-Oltra, J. Murga, M. Carda, J. A. Marco. Org. Lett. 2010, 12, 5752-5755.

  5. The high affinity dopamine uptake inhibitor, JHW 007, blocks cocaine-induced reward, locomotor stimulation and sensitization. C. Velázquez-Sánchez, A. Ferragud, J. Murga, M. Carda, J. J. Canales. European Neuropsychopharmacology, 2010, 20, 501-508.

  6. Stereoselective synthesis of the cytotoxic 14-membered macrolide aspergillide A. S. Díaz-Oltra, C. Angulo-Pachón, J. Murga, M. Carda, J. A. Marco. J. Org. Chem. 2010, 75, 1775-1778.

  7. A formal, stereoselective synthesis of the natural tetrahydropyran derivative ophiocerin D. J. Paños, J. Murga, M. Carda, J. A. Marco. Tetrahedron:Asymmetry 2010, 21, 425-428.

  8. Convergent, stereoselective syntheses of the glycosidase inhibitors broussonetines C, O and P. Celia Ribés, Eva Falomir, Juan Murga, Miguel Carda, J. Alberto Marco. Tetrahedron 2009, 65, 10612-10616.

  9. A Dopamine Transport Inhibitor with Markedly Low Abuse Liability Suppresses Cocaine Self-Administration in the Rat. A. Ferragud, C. Velázquez-Sánchez, V. Hernández-Rabaza, A. Nácher, J. Murga, M. Carda,  J. Canales. Psychopharmacology  2009, 207, 281-289.

  10. The Dopamine Uptake Inhibitor 3a-[bis(40-fluorophenyl)metoxy]-tropane Reduces Cocaine-Induced Early-Gene Expression, Locomotor Activity, and Conditioned Reward. C. Velázquez-Sánchez, A. Ferragud, V. Hernández-Rabaza, A. Nácher, V. Merino, M. Carda, J. Murga, J. J. Canales. Neuropsychopharmacology  2009, 34, 2497-2507.

  11. Stereoselective syntheses of the glycosidase inhibitors hyacinthacine A2, hyacinthacine A3 and 5-epi-hyacinthacine A3. C. Ribes, E. Falomir, M. Carda, J. A. Marco.Tetrahedron 2009, 65, 6965-6971.

  12. Stereoselective synthesis of the cytotoxic macrolide aspergillide B . S. Díaz-Oltra, C. A. Angulo-Pachón, M. N. Kneeteman, J. Murga, M. Carda, J. A. Marco. Tetrahedron Lett. 2009, 50, 3783-3785.

  13. Convergent, stereoselective syntheses of the glycosidase inhibitors broussonetines D and M. C. Ribes, E. Falomir, J. Murga, M. Carda, J. A. Marco. Org. Biomol. Chem. 2009, 7, 1355-1360.

  14. Stereoselective Synthesis of the Naturally Occurring Pyrrolidine Radicamine B and a Formal Synthesis of Nectrisine. C. Ribes, E. Falomir, M. Carda, J. A. Marco. J. Org. Chem. 2008, 73, 7779-7782.

  15. Double Diastereoselection in Aldol Reactions Mediated by Dicyclohexylchloroborane between L-Erythrulose Derivatives and Chiral α-Amino and α-Fluoro Aldehydes. Relative Importance of Felkin-Anh and Cornforth Transition States. S. Díaz-Oltra, M. Carda, J. Murga,  E. Falomir, J. A. Marco. Chem. Eur. J., 2008, 14, 9240-9254.

  16. Stereoselective Synthesis of the Naturally Occurring 2-Pyranone Dodoneine. P. Álvarez-Bercedo, E. Falomir, J. Murga, M. Carda, J. A. Marco. Eur. J. Org. Chem., 2008 , 73, 4015-4018.

  17. Stereoselective synthesis of the bacterial DNA primase inhibitor Sch 642305 and its C-4 epimer. J. García-Fortanet, M. Carda, A. Marco. Tetrahedron 2007, 63, 12131-12137.

  18. The Total Synthesis and Biological Properties of the Cytotoxic Macrolide FD-891 and its Non-Natural (Z)-C12 Isomer. J. García-Fortanet, J. Murga, M. Carda, J. A. Marco, R. Matesanz, J. F. Díaz. I. Barasoaín. Chem. Eur. J., 2007, 13, 5060-5074.

  19. Stereoselective synthesis of naturally occurring 5,6-dihydropyran-2-ones. J. A. Marco, M. Carda, J. Murga, y E. Falomir. Tetrahedron, 2007, 63, 2929-2958.

  20. Stereoselective synthesis of the glycosidase inhibitor australine through a one-pot, double-cyclization strategy . C. Ribes, E. Falomir, M. Carda y J. A. Marco. Org. Lett. 2007, 9, 77-80.

  21. Stereoselective synthesis of a C19-C26 fragment of amphidinolides G and H. P. Formentín, J. Murga, M. Carda y J. A. Marco. Tetrahedron: Asymmetry, 2006, 17, 2938-2942.

  22. Enantioselective synthesis and absolute configurations of aculeatins A, B, D, and 6-epi-aculeatin D. P. Álvarez-Bercedo, E. Falomir, M. Carda y J. A. Marco. Tetrahedron 2006, 62, 9641-9649.

  23. Stereoselective Synthesis of the Published Structure of Feigrisolide A. Structural Revision of Feigrisolides A and B. P. Álvarez-Bercedo, J. Murga, M. Carda y J. A. Marco. J. Org. Chem. 2006, 71, 5766-5769.

  24. Stereoselective Synthesis of the Cytotoxic Macrolide FD-891. J. García-Fortanet, J. Murga, M. Carda y J. A. Marco. Org. Lett. 2006, 8, 2695-2698.

  25. The Stereoselective Synthesis of the Nonnatural Enantiomers of Communiols A-C. A Stereochemical Correction. J. Murga, E. Falomir,  M. Carda y J. A. Marco. Nat. Prod. Commun. 2006, 1, 237-245.

  26. Antiparasite and antimycobacterial activity of passifloricin analogues.  W. Cardona, W. Quiñones, S. Robledo, I. Darío Vélez, J. Murga, J. García-Fortanet, M. Carda, D. Cardona y F. Echeverri. Tetrahedron 2006, 62, 4086-4092.

  27. Selective cleavage of acetals with ZnBr2 in dichlomethane. C. Ribes, E. Falomir y J. Murga. Tetrahedron 2006, 62, 1239-1244.

  28. Stereoselective Total Synthesis and Absolute Configuration of the Natural Decanolides (-)-Microcarpalide and (+)-Lethaloxin. The Identity of (+)-Lethaloxin and (+)-Pinolidoxin. J. García-Fortanet, J. Murga, E. Falomir, M. Carda  y  J. A. Marco. J. Org. Chem. 2005, 70, 9822-9827.

  29. Enantioselective synthesis and absolute configurations of aculeatins A and B. E. Falomir,  P. Álvarez-Bercedo, M. Carda y J. A. Marco. Tetrahedron Lett. 2005, 48, 8407-8410.

  30. Stereoselective synthesis of ent-communiols A-C.  J. Murga, E. Falomir,  M. Carda y J. A. Marco. Tetrahedron Lett. 2005, 46, 8199-8202.

  31. Double Diastereoselection in Aldol Reactions mediated by Dicyclohexylchloroborane between Chiral Aldehydes and A Chiral Ethyl Ketone Derived from L-Erythrulose . S. Díaz-Oltra, J. Murga, E. Falomir, M. Carda y J. A. Marco. J. Org. Chem. 2005, 70, 8130-8139.

  32. Stereoselective addition of organometallic reagents to a chiral acyclic nitrone derived from L-erythrulose. J. Murga, R. Portolés, E. Falomir,  M. Carda y J. A. Marco. Tetrahedron: Asymmetry 2005, 16, 1807-1816.

  33. Stereoselective synthesis of the published structure of synargentolide A and of one stereoisomer    thereof. J. García-Fortanet, J. Murga,  M. Carda y J. A. Marco. ARKIVOC 2005, part 9, 175-188.

  34. Stereoselective  Synthesis of the Naturally Occurring Styryllactones (+)-Goniofufurone and (+)-Cardiobutanolide.  P. Ruiz, J. Murga, M. Carda y J. A. Marco. J. Org. Chem. 2005, 70, 713-716.

  35. Stereoselective Synthesis of the C1-C12 fragment of the cytotoxic macrolide FD-891.  J. Murga, J. García-Fortanet,  M. Carda y J. A. Marco. Synlett 2004, 2830-2832.

  36. Stereoselective Synthesis of hyptolide and 6-epi-hyptolide.  J. García-Fortanet, J. Murga,  M. Carda y J. A. Marco. Tetrahedron 2004, 60, 12261-12267.

  37. Stereoselective Synthesis of the Antiprotozoal Lactone Passifloricin A and Seven Isomers Thereof. J. Murga, J. García-Fortanet,  M. Carda y J. A. Marco. J. Org. Chem. 2004, 69, 7277-7283.

  38. Stereoselective Synthesis of the C14-C26 fragment of the cytotoxic macrolide FD-891.  J. Murga, J. García-Fortanet,  M. Carda y J. A. Marco. Tetrahedron Lett. 2004, 45, 7499-7501.

  39. Stereoselective Synthesis of Anamarine. S. Díaz-Oltra, J. Murga, E. Falomir, M. Carda y J. A. Marco. Tetrahedron 2004, 60, 2979-2985.

  40. Stereoselective anti Aldol reactions of Erythrulose Derivatives. Functionalized Chiral d3 and d4 Synthons. J. Murga, P. Ruiz, E. Falomir, M. Carda, G. Peris y J. A. Marco. J. Org. Chem. 2004, 69, 1987-1992.

  41. Double Diastereoselection in Aldol Reactions mediated by Dicyclohexylchloroborane between Erythrulose Derivatives and Chiral Aldehydes. The Felkin-Anh vs. Cornforth dichotomy . J. A. Marco, M. Carda, S. Díaz-Oltra, J. Murga, E. Falomir  y H. Röper. J. Org. Chem. 2003, 68, 8577-8582.

  42. Asymmetric Synthesis of Passifloricin A: A Correction in Structure.  J. Murga, J. García-Fortanet,  M. Carda y J. A. Marco. Tetrahedron Lett. 2003, 44, 7909-7912.

  43. Stereoselective Synthesis and Determination of the Cytotoxic Properties of Spicigerolide and Three of Its Stereoisomers. E. Falomir, J. Murga, P. Ruiz, M. Carda, J. A. Marco, R. Pereda-Miranda, M. Fragoso-Serrano y C. M. Cerda-García-Rojas. J. Org. Chem. 2003, 68, 5672-5676.

  44. On the Structure of Passifloricin A: Asymmetric Synthesis of the d-Lactones of (2Z,5S,7R,9S,11S)- and (2Z,5R,7R,9S,11S)-Tetrahydroxyhexacos-2-enoic Acid.  J. García-Fortanet, J. Murga, M. Carda, J. A. Marco. Org. Lett. 2003, 10 , 1447-1449.

  45. Stereoselective synthesis of (+)-hyptolide. J. Murga, J. García-Fortanet, M. Carda, J. A. Marco. Tetrahedron Lett. 2003, 44, 1737-1739.

  46. Stereoselective synthesis of spicigerolide. E. Falomir, J. Murga, M. Carda y J. A. Marco. Tetrahedron Lett. 2003, 44, 539-541.

  47. Stereoselective synthesis of (-)-maliyngolide, (+)-malyngolide and (+)-tanikolide using ring-closing metathesis. M. Carda, S. Rodríguez, E. Castillo, A. Bellido, S. Díaz-Oltra y  J. A. Marco. Tetrahedron 2003, 59, 857-864.

  48. Erythrulose derivatives as functionalized chiral d3 and d4 synthons. J. Murga, E. Falomir,  M. Carda y  J. A. Marco. Tetrahedron Asymmetry 2002, 13 , 2317-2327.

  49. Influence of the Protecting Groups on the syn/anti Stereoselectivity of Boron Aldol Additions with Erythrulose Derivatives. A Theoretical and Experimental Study. J. Murga, E. Falomir, F. González, M. Carda y J. A. Marco. Tetrahedron 2002, 58 , 9697-9707.

  50. Stereoselective síntesis of microcarpalide. J. Murga, E. Falomir,. J. Garcia-Fortanet, M. Carda y J. A. Marco. Org. Lett. 2002, 4 , 3447-3449.

  51. Stereoselective synthesis of the naturally occurring lactones (-)-osmundalactone and (-)-muricatacine using ring-closing metathesis. M. Carda, S. Rodríguez, F. González, E. Castillo, A. Villanueva, J. A. Marco. Eur. J. Org. Chem. 2002, 2649-2655.

  52. Stereoselective synthesis of (-)-cytoxazone. M. Carda, F. González, R. Sánchez, J. A. Marco. Tetrahedron: Asymmetry 2002, 13, 1005-1010.

  53. Stereoselective Synthesis of (+)-Boronolide. M. Carda, S. Rodríguez, B. Segovia, J. A. Marco. J. Org. Chem. 2002, 67, 6560-6563.

  54. Synthesis of a,a-disubstituted a-amino acid derivatives in enantiopure form via stereoselective addition of Grignard reagents to a chiral acyclic nitrone derived from L-erythrulose. R. Portolés, J. Murga, E. Falomir, M. Carda, S. Uriel y J. A. Marco. Synlett 2002, 711-714.

  55. Synthesis of Conjugated d-Lactams Using Ring-Closing Metathesis. S. Rodríguez, E. Castillo, M. Carda, J. A. Marco. Tetrahedron 2002, 58, 1185-1192.

  56. Stereoselective Allylations of Erythrulose Derivatives Under Anhydrous Conditions. M. Carda, E. Castillo, S. Rodríguez, F. González, J. A. Marco. Tetrahedron: Asymmetry 2001, 12, 1417-1429.

  57. An ab initio Study of the Enolboration of 3-Pentanone Mediated by Boron Monochlorides L2BCl. J. Murga, E. Falomir, M. Carda y J. A. Marco. Tetrahedron 2001, 57, 6239-6247.

  58. Chlorodicyclohexylborane-Mediated Aldol Additions of a,a´-Dioxygenated Ketones. J. Murga, E. Falomir, M. Carda, F. González y J. A. Marco. Org. Lett. 2001, 3, 901-904.

  59. Stereoselective 1,3-Dipolar Cycloadditions of a Chiral Nitrone Derived from Erythrulose. An Experimental and DFT Theoretical Study. M. Carda, R. Portolés, J. Murga, S. Uriel, J. A. Marco, L. R. Domingo, R. J. Zaragozá y H. Röper. J. Org. Chem. 2000, 65, 7000-7009.

  60. Stereoselective Synthesis of syn-a-methyl-b-hydroxy Esters. M. Carda, J. Murga, E. Falomir, F. González y J. A. Marco. Tetrahedron Asymmetry 2000, 11, 3211-3220.

  61. A stereoselective synthesis of (+)-malyngolide via a ring-closing olefin metathesis. M. Carda , E. Castillo, S. Rodríguez, J. A. Marco. Tetrahedron Lett. 2000, 41, 5511-5513.

  62. Aldol reactions with Erytrulose Derivatives: Stereoselective Synthesis of Differentially Protected syn-a-b-Dihydroxy Esters. M. Carda, J. Murga, E. Falomir, F. González y J. A. Marco. Tetrahedron 2000,  56, 677-683.

 

© 2011 Grupo de Síntesis Orgánica. Universidad Jaume I