Publicaciones en las que colabora con Alma Viso Beronda (47)

2017

  1. Chiral Sulfur Functional Groups as Definers of the Chirality at the Metal in Ir and Rh Half-Sandwich Complexes: A Combined CD/X-ray Study

    Chemistry - A European Journal, Vol. 23, Núm. 58, pp. 14523-14531

  2. Desulfinylation of Ag(I) Sulfinyl Mesoionic Carbenes: Preparation of C-Unsubstituted Au(I)-1,2,3-Triazole Carbene Complexes

    Organic Letters, Vol. 19, Núm. 4, pp. 822-825

  3. Development of a Nucleotide Exchange Inhibitor That Impairs Ras Oncogenic Signaling

    Chemistry - A European Journal, Vol. 23, Núm. 7, pp. 1676-1685

  4. Gold(I)-Catalyzed Cycloisomerization-Dimerization Cascade of Benzene-Tethered 1,6-Enynes

    Journal of Organic Chemistry, Vol. 82, Núm. 14, pp. 7546-7554

  5. Sulfur Groups Improve the Performance of Triazole- and Triazolium-Based Interaction Units in Anion Binding

    Journal of Organic Chemistry, Vol. 82, Núm. 6, pp. 3341-3346

2016

  1. Gold Sulfinyl Mesoionic Carbenes: Synthesis, Structure, and Catalytic Activity

    Organic Letters, Vol. 18, Núm. 15, pp. 3570-3573

2011

  1. Development of non-peptide ligands of growth factor receptor-bound protein 2-src homology 2 domain using molecular modeling and NMR spectroscopy

    Journal of Medicinal Chemistry, Vol. 54, Núm. 4, pp. 1096-1100

2010

  1. Development of fluorescent ligands for the human 5-HT1A receptor

    ACS Medicinal Chemistry Letters, Vol. 1, Núm. 6, pp. 249-253

  2. Development of molecular probes for the human 5-HT6 receptor

    Journal of Medicinal Chemistry, Vol. 53, Núm. 19, pp. 7095-7106

2008

  1. The medicinal chemistry of agents targeting monoacylglycerol lipase

    Current Topics in Medicinal Chemistry, Vol. 8, Núm. 3, pp. 231-246

2006

  1. Synthesis of highly substituted enantiopure piperazines and ketopiperazines from vicinal N-sulfinyl diamines

    Journal of Organic Chemistry, Vol. 71, Núm. 4, pp. 1442-1448

2005

  1. Activation of the endocannabinoid system as therapeutic approach in a murine model of multiple sclerosis

    FASEB Journal, Vol. 19, Núm. 10, pp. 1338-1340

  2. Highly diastereoselective [3+2] cycloadditions between non-racemic p-tolylsulfinimines and iminoesters: An efficient entry to enantiopure imidazolidines and vicinal diaminoalcohols

    Phosphorus, Sulfur and Silicon and the Related Elements

  3. Involvement of cannabinoids in cellular proliferation

    Mini-Reviews in Medicinal Chemistry

  4. Synthesis and structure-activity relationships of a new model of arylpiperazines. 8. Computational simulation of ligand-receptor interaction of 5-HT1AR agonists with selectivity over α1- adrenoceptors

    Journal of Medicinal Chemistry, Vol. 48, Núm. 7, pp. 2548-2558

2004

  1. Characterization of an anandamide degradation system in prostate epithelial PC-3 cells: Synthesis of new transporter inhibitors as tools for this study

    British Journal of Pharmacology, Vol. 141, Núm. 3, pp. 457-467

  2. Comparison of anandamide transport in FAAH wild-type and knockout neurons: Evidence for contributions by both FAAH and the CB1 receptor to anandamide uptake

    Biochemistry, Vol. 43, Núm. 25, pp. 8184-8190

  3. Fine-Tuned Aminal Cleavage: A Concise Route to Differentially Protected Enantiopure syn-α,β-Diamino Esters

    Journal of Organic Chemistry, Vol. 69, Núm. 5, pp. 1542-1547

  4. Synthesis and structure-activity relationships of a new model of arylpiperazines. Part 7: Study of the influence of lipophilic factors at the terminal amide fragment on 5-HT1A affinity/selectivity

    Bioorganic and Medicinal Chemistry, Vol. 12, Núm. 6, pp. 1551-1557

2003

  1. Design and synthesis of S-(-)-2-[[4-(napht-1-yl)piperazin-1-yl]methyl]-1,4-dioxoperhydropyrrolo[1,2- a]pyrazine (CSP-2503) using computational simulation. A 5-HT1A receptor agonist

    Bioorganic and Medicinal Chemistry Letters, Vol. 13, Núm. 8, pp. 1429-1432