Publicaciones (89) Publicaciones de JUAN FRANCISCO SANZ CERVERA

2018

  1. Arylureas derived from colchicine: Enhancement of colchicine oncogene downregulation activity

    European Journal of Medicinal Chemistry, Vol. 150, pp. 817-828

  2. Selective targeting of collagen IV in the cancer cell microenvironment reduces tumor burden

    Oncotarget, Vol. 9, Núm. 13, pp. 11020-11045

  3. Synthesis and biological evaluation of cyclic derivatives of combretastatin A-4 containing group 14 elements

    Organic and Biomolecular Chemistry, Vol. 16, Núm. 32, pp. 5859-5870

2017

  1. Identification of the Iodination and Bromination Products of 3-Hydroxybenzaldehyde: Preparation of 5-Hydroxy-2-iodobenzaldehyde

    Organic Preparations and Procedures International, Vol. 49, Núm. 3, pp. 265-272

2016

  1. Design, synthesis and antimalarial evaluation of novel thiazole derivatives

    Bioorganic and Medicinal Chemistry Letters, Vol. 26, Núm. 16, pp. 3938-3944

2009

  1. Cross-metathesis reactions as an efficient tool in the synthesis of fluorinated cyclic β-amino acids

    Journal of Organic Chemistry, Vol. 74, Núm. 9, pp. 3414-3423

  2. Fluorous TBAF: A convenient and selective reagent for fluoride-mediated deprotections

    Journal of Organic Chemistry, Vol. 74, Núm. 16, pp. 6398-6401

  3. New fluorinated peptidomimetics through tandem aza-michael addition to α-trifluoromethyl acrylamide acceptors: Synthesis and conformational study in solid state and solution

    Journal of Organic Chemistry, Vol. 74, Núm. 8, pp. 3122-3132

  4. New fluorinated pyrazol and uracil derivatives: Synthesis and biological activity

    ACS Symposium Series

  5. Nitrogen-containing organofluorine derivatives: An overview

    Synlett, pp. 525-549

  6. Organocatalytic anti/-selective mannich reactions with fluorinated aldimines: synthesis of anti-γ-fluoroalkyl-γ-amino alcohols

    European Journal of Organic Chemistry, pp. 5208-5214

  7. Recent advances in the synthesis of pyrazoles. A review

    Organic Preparations and Procedures International, Vol. 41, Núm. 4, pp. 253-290

  8. Solution versus fluorous versus solid-phase synthesis of 2,5-disubstituted 1,3-azoles. Preliminary antibacterial activity studies

    Journal of Organic Chemistry, Vol. 74, Núm. 23, pp. 8988-8996

2008

  1. An efficient entry to optically active anti- and syn-β-amino-α- trifluoromethyl alcohols

    Organic Letters, Vol. 10, Núm. 4, pp. 605-608

  2. An efficient synthesis of uracil derivatives from 2-alkyl-Δ2-oxazolines and nitriles

    Journal of Fluorine Chemistry, Vol. 129, Núm. 9, pp. 836-847

  3. Improved regioselectivity in pyrazole formation through the use of fluorinated alcohols as solvents: Synthesis and biological activity of fluorinated tebufenpyrad analogs

    Journal of Organic Chemistry, Vol. 73, Núm. 9, pp. 3523-3529

  4. Solution-, solid-phase, and fluorous synthesis of β,β- difluorinated cyclic quaternary a-amino acid derivatives: A comparative study

    Chemistry - A European Journal, Vol. 14, Núm. 23, pp. 7019-7029

  5. Synthesis of new fluorinated tebufenpyrad analogs with acaricidal activity through regioselective pyrazole formation

    Journal of Organic Chemistry, Vol. 73, Núm. 21, pp. 8545-8552

  6. Tiratricol neutralizes bacterial endotoxins and reduces lipopolysaccharide-induced TNF-α production in the cell

    Chemical Biology and Drug Design, Vol. 72, Núm. 4, pp. 320-328

2007

  1. Asymmetric synthesis of fluorinated amino macrolactones through ring-closing metathesis

    Journal of Organic Chemistry, Vol. 72, Núm. 23, pp. 8716-8723