Publicaciones en colaboración con investigadores/as de King Saud University (18)

2021

  1. Synthesis of Fused Quinoline Derivatives from Easily Accessible N-(2-aminobenzylidene)-4-methylanilines under Catalyst-Free Conditions in Water

    ChemistrySelect, Vol. 6, Núm. 38, pp. 10436-10439

2019

  1. D-Ring-Modified Analogues of Luotonin A with Reduced Planarity: Design, Synthesis, and Evaluation of Their Topoisomerase Inhibition-Associated Cytotoxicity

    BioMed Research International, Vol. 2019

  2. Design and synthesis of A- and D ring-modified analogues of luotonin A with reduced planarity

    Tetrahedron Letters, Vol. 60, Núm. 23, pp. 1514-1517

  3. Multicomponent domino protocol for the stereoselective synthesis of novel pyrrolo[3,2-c]quinolinone hybrid heterocycles

    Tetrahedron Letters, Vol. 60, Núm. 8, pp. 602-605

  4. Spirooxindole-pyrrolidine heterocyclic hybrids promotes apoptosis through activation of caspase-3

    Bioorganic and Medicinal Chemistry, Vol. 27, Núm. 12, pp. 2487-2498

2018

  1. Highly functionalized pyrrolidine analogues: stereoselective synthesis and caspase-dependent apoptotic activity

    RSC Advances, Vol. 8, Núm. 72, pp. 41226-41236

  2. Multicomponent domino synthesis, anticancer activity and molecular modeling simulation of complex dispirooxindolopyrrolidines

    Molecules, Vol. 23, Núm. 5

  3. Regio and stereoselective synthesis of anticancer spirooxindolopyrrolidine embedded piperidone heterocyclic hybrids derived from one-pot cascade protocol

    Chemistry Central Journal, Vol. 12, Núm. 1

  4. Regio- and diastereoselective synthesis of anticancer spirooxindoles derived from tryptophan and histidine via three-component 1,3-dipolar cycloadditions in an ionic liquid

    Tetrahedron, Vol. 74, Núm. 38, pp. 5358-5366

2017

  1. Design, synthesis and antiproliferative activity of decarbonyl luotonin analogues

    European Journal of Medicinal Chemistry, Vol. 138, pp. 932-941

2016

  1. A sustainable approach to the stereoselective synthesis of diazaheptacyclic cage systems based on a multicomponent strategy in an ionic liquid

    Molecules, Vol. 21, Núm. 2

  2. Erratum to: Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (Autophagy, 12, 1, 1-222, 10.1080/15548627.2015.1100356

    Autophagy

  3. Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

    Autophagy, Vol. 12, Núm. 1, pp. 1-222

2015

  1. An expedient regio- and diastereoselective synthesis of hybrid frameworks with embedded spiro[9,10]dihydroanthracene [9,3']-pyrrolidine and Spiro[oxindole-3,2'-pyrrolidine] motifs via an ionic liquid-mediated multicomponent reaction

    Molecules, Vol. 20, Núm. 9, pp. 16142-16153

  2. Dipolar Cycloaddition-Based Multicomponent Reactions in Ionic Liquids: A Green, Fully Stereoselective Synthesis of Novel Polycyclic Cage Systems with the Generation of Two New Azaheterocyclic Rings

    Synthesis (Germany), Vol. 47, Núm. 18, pp. 2721-2730

  3. Straightforward synthesis of pyrrolo[3,4-b]quinolines through intramolecular Povarov reactions

    Tetrahedron Letters, Vol. 56, Núm. 49, pp. 6900-6903

2012

  1. Domino reactions in water: Diastereoselective synthesis of densely functionalized indolyldihydrofuran derivatives

    Green Chemistry, Vol. 14, Núm. 3, pp. 750-757

  2. Nuclear ribosomal internal transcribed spacer (ITS) region as a universal DNA barcode marker for Fungi

    Proceedings of the National Academy of Sciences of the United States of America, Vol. 109, Núm. 16, pp. 6241-6246