JOSÉ RAMÓN
SUÁREZ ÁLVAREZ
Profesor ayudante doctor
Argitalpenak (26) JOSÉ RAMÓN SUÁREZ ÁLVAREZ argitalpenak
2024
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Design and sustainable synthesis of small mannose-based glycodendrons as ligands for HIV-1 envelope protein gp120: Toward an explanation for their binding
Catalysis Today, Vol. 429
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Exploring Rigid and Flexible Scaffolds to Develop Potent Glucuronic Acid Glycodendrimers for Dengue Virus Inhibition
Bioconjugate Chemistry, Vol. 35, Núm. 1, pp. 34-42
2023
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Evaluation of Anti-Neuroinflammatory Activity of Isatin Derivatives in Activated Microglia
Molecules, Vol. 28, Núm. 12
2021
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Discovery of 5-{2-[5-Chloro-2-(5-ethoxyquinoline-8-sulfonamido)phenyl]ethynyl}-4-methoxypyridine-2-carboxylic Acid, a Highly Selective in Vivo Useable Chemical Probe to Dissect MCT4 Biology
Journal of Medicinal Chemistry, Vol. 64, Núm. 16, pp. 11904-11933
2016
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Efficient multi-click approach to well-defined two-faced octasilsesquioxanes: The first perfect Janus nanocube
Chemical Communications, Vol. 52, Núm. 34, pp. 5792-5795
2015
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Editorial (Thematic Issue: Advances in Organocatalytic Chemistry)
Current Organocatalysis, Vol. 2, Núm. 2, pp. 78-78
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Nonafluorobutanesulfonyl Azide as a Shelf-Stable Highly Reactive Oxidant for the Copper-Catalyzed Synthesis of 1,3-Diynes from Terminal Alkynes
Journal of Organic Chemistry, Vol. 80, Núm. 2, pp. 1098-1106
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Nucleophilic addition of amines to ruthenium carbenes: Ortho-(alkynyloxy)benzylamine cyclizations towards 1,3-benzoxazines
Angewandte Chemie - International Edition, Vol. 54, Núm. 9, pp. 2724-2728
2013
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One-pot synthesis of 2,3,4,5,6-pentasubstituted tetrahydropyrans using lithiation–borylation, allylation and Prins cyclisation reactions
Tetrahedron Letters, Vol. 54, Núm. 1, pp. 49-51
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Rhodium-catalyzed intermolecular C–H amination of simple hydrocarbons using the shelf-stable nonafluorobutanesulfonyl azide
Chemical Communications, Vol. 49, Núm. 80, pp. 9194-9196
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Synthesis of N,N′‐Disulfonylamidines from Sulfonamides and Alkynes by a Two‐Step, One‐Pot Reaction with Nonafluorobutanesulfonyl Azide
Advanced Synthesis & Catalysis, Vol. 355, Núm. 5, pp. 913-918
2011
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Synthesis of α‐Diazo Carbonyl Compounds with the Shelf‐Stable Diazo Transfer Reagent Nonafluorobutanesulfonyl Azide
Advanced Synthesis & Catalysis, Vol. 353, Núm. 4, pp. 575-579
2010
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Application of the Lithiation−Borylation Reaction to the Preparation of Enantioenriched Allylic Boron Reagents and Subsequent In Situ Conversion into 1,2,4-Trisubstituted Homoallylic Alcohols with Complete Control over All Elements of Stereochemistry
Journal of the American Chemical Society, Vol. 132, Núm. 11, pp. 4025-4028
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Nonafluorobutanesulfonyl azide: A shelf-stable diazo transfer reagent for the synthesis of azides from primary amines
Advanced Synthesis and Catalysis, Vol. 352, Núm. 14-15, pp. 2515-2520
2009
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The fate of the tert-butylsulfinyl auxiliary after acid-promoted cleavage—a method for recycling t-BuSONH2
Tetrahedron Letters, Vol. 50, Núm. 26, pp. 3482-3484
2007
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Ring opening of chiral 2-(1-aminoalkyl)epoxides by aliphatic thiols with total selectivity: synthesis of enantiopure 3-amino-1-(alkylthio)alkan-2-ols
Tetrahedron, Vol. 63, Núm. 13, pp. 2805-2810
2006
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Synthesis of enantiopure (αS,βS)- or (αR,βS)-β- amino alcohols by complete regioselective opening of aminoepoxides by organolithium reagents LiAlH4 or LiAlD4
Journal of Organic Chemistry, Vol. 71, Núm. 17, pp. 6420-6426
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Synthesis of enantiopure allylamines by reductive alkylation of amino epoxides with organolithium reagents
Organic Letters, Vol. 8, Núm. 2, pp. 349-351
2005
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Regioselective ring opening of amino epoxides with nitriles: An easy synthesis of (2R,3S)- and (2S,3S)-1,3-diaminoalkan-2-ols with differently protected amine functions
Journal of Organic Chemistry, Vol. 70, Núm. 18, pp. 7447-7450
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Selective ring-opening of nonactivated amino aziridines by thiols and unusual nucleophilic substitution of a dibenzylamino group
Journal of Organic Chemistry, Vol. 70, Núm. 23, pp. 9411-9416