Alma Viso
0000-0003-2622-4777
CSIC
84 papers found
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[2,3]-Sigmatropic Rearrangements of 3-Sulfinyl Dihydropyrans: Application to the Syntheses of the Cores ofent-Dysiherbaine and Deoxymalayamicin A
Highly Diastereoselective Addition of Lithio Vinyl Sulfoxides toN-Sulfinimines: An Entry to Enantiopure 3-Sulfinyl-2,5-cis-dihydropyrroles
Sulfur-Directed Enantioselective Synthesis of Functionalized Dihydropyrans
The Medicinal Chemistry of Agents Targeting Monoacylglycerol Lipase
Formal synthesis of ent-dysiherbaine from sulfinyl dihydropyrans by sigmatropic rearrangement and tethered aminohydroxylation
Synthesis of Enantiopure Vicinal Diaminoesters and Ketopiperazines from N-Sulfinylimidazolidines.
Highly Diastereoselective Staudinger Reaction on 5,6-Dihydropyrazin-2-(1H)-ones. Synthesis of Enantiopure Fused Oxopiperazino-β-lactams.
Nucleophilic epoxidation of γ-alkoxy dienyl sulfoxide derivatives
Synthesis of Highly Substituted Enantiopure Piperazines and Ketopiperazines from VicinalN-Sulfinyl Diamines
Metal-Catalyzed Oxidation and Epoxidation of α-Hydroxy Vinyl and Dienyl Sulfoxides
Sulfur-Mediated Synthesis of Substituted Tetrahydrofurans: Application to the Synthesis of Goniofufurone
Sulfur Participation in [3,3]-Sigmatropic Rearrangements
Synthesis of Tetrahydrofurfurylamines Related to Muscarine
Reductive Cleavage of Tetrahydrofuryl Sulfur-Substituted Oxiranes: Application to the Formal Synthesis of Kumausyne and Kumausallene
Highly Diastereoselective Diels—Alder Reactions with Enantiopure Sulfinyl-Substituted 1-Hydroxymethyldienes.
α,β-Diamino Acids: Biological Significance and Synthetic Approaches
Synthesis and Structure−Activity Relationships of a New Model of Arylpiperazines. 8.1Computational Simulation of Ligand−Receptor Interaction of 5-HT1AR Agonists with Selectivity over α1-Adrenoceptors
Synthesis of Functionalized Tetrahydrofurans from Hydroxy Sulfinyl Dienes
Involvement of Cannabinoids in Cellular Proliferation
Sulfoxide-controlled SN2′ displacements between cuprates and vinyl and alkynyl epoxy sulfoxides
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