Works matching AU Leonelli, Francesca
Results: 29
Selective Interaction of Chiral Carbon Dots with Nucleic Acids: A Promising Nanosensing Platform.
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- Chemistry - A European Journal, 2024, v. 30, n. 70, p. 1, doi. 10.1002/chem.202402787
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Targeting the Antifungal Activity of Carbon Dots against Candida albicans Biofilm Formation by Tailoring Their Surface Functional Groups.
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- Chemistry - A European Journal, 2024, v. 30, n. 18, p. 1, doi. 10.1002/chem.202303631
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Organocatalyst Design for the Stereoselective Annulation towards Bicyclic Diketones and Analogues.
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- Symmetry (20738994), 2022, v. 14, n. 2, p. N.PAG, doi. 10.3390/sym14020355
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Two Different Models to Predict Ionic-Liquid Diffraction Patterns: Fixed-Charge versus Polarizable Potentials.
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- ChemPhysChem, 2015, v. 16, n. 1, p. 197, doi. 10.1002/cphc.201402577
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Transamidation‐based vitrimers from renewable sources.
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- Journal of Applied Polymer Science, 2022, v. 139, n. 25, p. 1, doi. 10.1002/app.52408
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Chiral HPLC Resolution of the Wieland–Miescher Ketone and Derivatives.
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- Journal of Liquid Chromatography & Related Technologies, 2003, v. 26, n. 3, p. 409, doi. 10.1081/JLC-120017179
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Rice Phytoalexins: Half a Century of Amazing Discoveries; Part I: Distribution, Biosynthesis, Chemical Synthesis, and Biological Activities.
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- Plants (2223-7747), 2023, v. 12, n. 2, p. 260, doi. 10.3390/plants12020260
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Impact of Environmental Factors on Stilbene Biosynthesis.
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- Plants (2223-7747), 2021, v. 10, n. 1, p. 90, doi. 10.3390/plants10010090
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Sea Surface Temperature Intercomparison in the Framework of the Copernicus Climate Change Service (C3S).
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- Journal of Climate, 2021, v. 34, n. 13, p. 5257, doi. 10.1175/JCLI-D-20-0793.1
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Click‐Connected 2‐(Hydroxyimino)aldehydes for the Design of UV‐Responsive Functional Molecules.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 2, p. 289, doi. 10.1002/ejoc.202001303
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Enantioselective Synthesis and X‐ray Structure of (+)((4aS,5S,8aS)‐5,8a‐Dimethyl‐7‐methyleneoctahydro‐2H‐spiro[naphthalene‐1,2′‐[1,3]dioxolan]‐5‐yl)methyl‐4‐iodobenzoate.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 7, p. 1594, doi. 10.1002/ejoc.201801771
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Carbon Dots as Bioactive Antifungal Nanomaterials.
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- ChemMedChem, 2024, v. 19, n. 23, p. 1, doi. 10.1002/cmdc.202400463
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Self-Healing and Reprocessable Oleic Acid-Based Elastomer with Dynamic S-S Bonds as Solvent-Free Reusable Adhesive on Copper Surface.
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- Polymers (20734360), 2022, v. 14, n. 22, p. 4919, doi. 10.3390/polym14224919
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Targeting Serotonin 2A and Adrenergic α<sub>1</sub> Receptors for Ocular Antihypertensive Agents: Discovery of 3,4‐Dihydropyrazino[1,2‐b]indazol‐1(2H)‐one Derivatives.
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- ChemMedChem, 2018, v. 13, n. 15, p. 1597, doi. 10.1002/cmdc.201800199
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Unexpected Racemization in the Course of the Acetalization of (+)-(S)-5-Methyl-Wieland–Miescher Ketone with 1,2-Ethanediol and TsOH under Classical Experimental Conditions.
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- International Journal of Molecular Sciences, 2019, v. 20, n. 24, p. 6147, doi. 10.3390/ijms20246147
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Stemarane Diterpenes and Diterpenoids †.
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- International Journal of Molecular Sciences, 2019, v. 20, n. 11, p. 2627, doi. 10.3390/ijms20112627
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Chlamydomonas reinhardtii : A Factory of Nutraceutical and Food Supplements for Human Health.
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- Molecules, 2023, v. 28, n. 3, p. 1185, doi. 10.3390/molecules28031185
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N -Acetyl-l-phenylalanine Racemization during TBTU Amidation: An In-Depth Study for the Synthesis of Anti-Inflammatory 2-(N -Acetyl)-l-phenylalanylamido-2-deoxy-d-glucose (NAPA).
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- Molecules, 2023, v. 28, n. 2, p. 581, doi. 10.3390/molecules28020581
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Stemodane Diterpenes and Diterpenoids: Isolation, Structure Elucidation, Biogenesis, Biosynthesis, Biological Activity, Biotransformations, Metabolites and Derivatives Biological Activity, Rearrangements †.
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- Molecules, 2021, v. 26, n. 9, p. 2761, doi. 10.3390/molecules26092761
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(+)-Podocarpic Acid as Chiral Template in the Synthesis of Aphidicolane, Stemodane and Stemarane Diterpenoids.
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- Molecules, 2016, v. 21, n. 9, p. 1197, doi. 10.3390/molecules21091197
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Application of microemulsions for the removal of synthetic resins from paintings on canvas.
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- Natural Product Research, 2019, v. 33, n. 7, p. 1015, doi. 10.1080/14786419.2016.1244191
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- Article
Synthesis of (+)-13-Stemarene and (+)-18-Deoxystemarin: Expeditious Preparation of the Key 6-exo-Hydroxybicyclo2.2.2octan-2-oneEthylene Dithioacetal The numbering refers to the bicyclo2.2.2octane moiety and will be used throughout the text.
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- Helvetica Chimica Acta, 2008, v. 91, n. 4, p. 0, doi. 10.1002/hlca.200890063
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A New and Simply Available Class of Hydrosoluble Bioconjugates by Coupling Paclitaxel to Hyaluronic Acid through a 4-Hydroxybutanoic Acid Derived Linker.
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- Helvetica Chimica Acta, 2005, v. 88, n. 1, p. 154
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A New Preparation of 1,3,3-Trimethylbicyclo[2.2.2]octan-2,6-dione, a Never Isolated Intermediate in a Total Synthesis of (+)-Norpatchoulenol. Formal Total Synthesis of (±)-Iso-Norpatchoulenol.
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- Helvetica Chimica Acta, 2004, v. 87, n. 8, p. 2120
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The Formation of 8-Epipodocarp-9(11)en-12-one in the Course of the Preparation of Podocarp-9(11)-en-12-one from O-Methylpodocarpane and Related Studies.
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- Helvetica Chimica Acta, 2002, v. 85, n. 9, p. 2817, doi. 10.1002/1522-2675(200209)85:9<2817::AID-HLCA2817>3.0.CO;2-7
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New Evidence of Mediterranean Climate Change and Variability from Sea Surface Temperature Observations.
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- Remote Sensing, 2020, v. 12, n. 1, p. 132, doi. 10.3390/rs12010132
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A Highly Efficient and Stereocontrolled Synthesis of 2-Deoxy-1,5-thioanhydro-L-hexitols from D-Glycals in a Tandem Nucleophilic Displacement Reaction.
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- European Journal of Organic Chemistry, 2006, v. 2006, n. 14, p. 3097, doi. 10.1002/ejoc.200600010
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Stereoselective Michael-Type Addition of Organocopper Reagents to Enones Derived from Glycals in the Synthesis of 2-Phosphono-a-C-Glycosides.
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- European Journal of Organic Chemistry, 2005, v. 2005, n. 13, p. 2671, doi. 10.1002/ejoc.200500149
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Neighboring-Group Participation in Nitrile-Forming Beckmann Fragmentation Reactions: Synthesis of Enantiopure (E)-2,3-Di-O-substituted-5-methoxy- pent-4-enenitriles and Their Conversion into Pyranosylamines.
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- European Journal of Organic Chemistry, 2004, v. 2004, n. 24, p. 5083, doi. 10.1002/ejoc.200400498
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