Publicacións nas que colabora con SANTIAGO DIAZ OLTRA (20)

2015

  1. Inhibitory effect of pironetin analogue/colchicine hybrids on the expression of the VEGF, hTERT and c-Myc genes

    Bioorganic and Medicinal Chemistry Letters, Vol. 25, Núm. 16, pp. 3194-3198

  2. The Mechanism of the Interactions of Pironetin Analog/Combretastatin A-4 Hybrids with Tubulin

    Archiv der Pharmazie, Vol. 348, Núm. 8, pp. 541-547

2014

  1. Design and synthesis of pironetin analogue/colchicine hybrids and study of their cytotoxic activity and mechanisms of interaction with tubulin

    Journal of Medicinal Chemistry, Vol. 57, Núm. 24, pp. 10391-10403

  2. Design and synthesis of pironetin analogue/combretastatin A-4 hybrids and evaluation of their cytotoxic activity

    European Journal of Organic Chemistry, Vol. 2014, Núm. 11, pp. 2284-2296

  3. Design and synthesis of pironetin analogue/combretastatin A-4 hybrids containing a 1,2,3-triazole ring and evaluation of their cytotoxic activity

    European Journal of Medicinal Chemistry, Vol. 87, pp. 125-130

2013

  1. Stereoselective synthesis of a C1-C18 fragment of amphidinolides G and H

    Tetrahedron, Vol. 69, Núm. 15, pp. 3192-3196

  2. Synthesis and biological evaluation as microtubule-active agents of several tetrahydrofuran and spiroacetal derivatives

    Current Medicinal Chemistry, Vol. 20, Núm. 9, pp. 1173-1182

  3. Synthesis and biological evaluation of truncated α-tubulin-binding pironetin analogues lacking alkyl pendants in the side chain or the dihydropyrone ring

    Organic and Biomolecular Chemistry, Vol. 11, Núm. 35, pp. 5809-5826

  4. Synthesis and biological evaluation of α-tubulin-binding pironetin analogues with enhanced lipophilicity

    European Journal of Organic Chemistry, pp. 1116-1123

  5. Synthesis of combretastatin A-4 O-alkyl derivatives and evaluation of their cytotoxic, antiangiogenic and antitelomerase activity Dedicated to Professor G. Asensio, University of Valencia, on the occasion of his 65th birthday

    Bioorganic and Medicinal Chemistry, Vol. 21, Núm. 23, pp. 7267-7274

2012

  1. Double diastereoselection in anti aldol reactions mediated by dicyclohexylchloroborane between an l-erythrulose derivative and chiral aldehydes

    Organic and Biomolecular Chemistry, Vol. 10, Núm. 34, pp. 6937-6944

2011

  1. Synthesis and biological properties of the cytotoxic 14-membered macrolides aspergillide A and B

    Chemistry - A European Journal, Vol. 17, Núm. 2, pp. 675-688

2010

  1. Stereoselective synthesis and structural correction of the naturally occurring lactone stagonolide G

    Organic Letters, Vol. 12, Núm. 24, pp. 5752-5755

  2. Stereoselective synthesis of the cytotoxic 14-membered macrolide aspergillide a

    Journal of Organic Chemistry, Vol. 75, Núm. 5, pp. 1775-1778

2009

  1. Stereoselective synthesis of the cytotoxic macrolide aspergillide B

    Tetrahedron Letters, Vol. 50, Núm. 27, pp. 3783-3785

2008

  1. Aldol reactions between L-erythrulose derivatives and chiral α-amino and α-fluoro aldehydes: Competition between felkin-anh and cornforth transition states

    Chemistry - A European Journal, Vol. 14, Núm. 30, pp. 9240-9254

2005

  1. 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 A1α

    Journal of Organic Chemistry, Vol. 70, Núm. 20, pp. 8130-8139

2004

  1. Stereoselective synthesis of anamarine

    Tetrahedron, Vol. 60, Núm. 13, pp. 2979-2985

2003

  1. Double Diastereoselection in Aldol Reactions Mediated by Dicyclohexylchloroborane between L-Erythrulose Derivatives and Chiral Aldehydes. The Felkin-Anh versus Cornforth Dichotomy

    Journal of Organic Chemistry, Vol. 68, Núm. 22, pp. 8577-8582

  2. Stereoselective synthesis of (-)-malyngolide, (+)-malyngolide and (+)-tanikolide using ring-closing metathesis

    Tetrahedron, Vol. 59, Núm. 6, pp. 857-864