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The top documents of ugo-chiacchio

Diastereoselective Synthesis of N,O-Psiconucleosides, a New Class of Modified Nucleosides
Diastereoselective Synthesis of N,O-Psiconucleosides, a New Class of Modified Nucleosides
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ChemInform Abstract: Stereoselective Synthesis of Enantiomerically Pure Isoxazolidine-Fused δ-Lactams
ChemInform Abstract: Stereoselective Synthesis of Enantiomerically Pure Isoxazolidine-Fused δ-Lactams
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ChemInform Abstract: Diastereoselective and Enantioselective Synthesis of 4′-Aza Analogues of 2′,3′-Dideoxynucleosides
ChemInform Abstract: Diastereoselective and Enantioselective Synthesis of 4′-Aza Analogues of 2′,3′-Dideoxynucleosides
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ChemInform Abstract: Stereoselective Synthesis of Homochiral Annulated Sultams via Intramolecular Cycloaddition Reactions
ChemInform Abstract: Stereoselective Synthesis of Homochiral Annulated Sultams via Intramolecular Cycloaddition Reactions
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Intramolecular Cycloadditions of α-Allyloxycarbonylnitrones: Stereoselective Synthesis of 3-Amino-2(5H)furanones
Intramolecular Cycloadditions of α-Allyloxycarbonylnitrones: Stereoselective Synthesis of 3-Amino-2(5H)furanones
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Isoxazolidine Analogues of Pseudouridine: A New Class of Modified Nucleosides
Isoxazolidine Analogues of Pseudouridine: A New Class of Modified Nucleosides
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Synthesis of Pyrimidine-Containing 3-Aminobutenolides
Synthesis of Pyrimidine-Containing 3-Aminobutenolides
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ChemInform Abstract: Cycloaddition Methodology. A Useful Entry Towards Biologically Active Heterocycles
ChemInform Abstract: Cycloaddition Methodology. A Useful Entry Towards Biologically Active Heterocycles
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ChemInform Abstract: Cycloaddition Methodology: A Useful Entry Towards Heterocyclic Systems
ChemInform Abstract: Cycloaddition Methodology: A Useful Entry Towards Heterocyclic Systems
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Synthesis of Methyleneisoxazolidine Nucleoside Analogues by Microwave-Assisted Nitrone Cycloaddition
Synthesis of Methyleneisoxazolidine Nucleoside Analogues by Microwave-Assisted Nitrone Cycloaddition
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13C NMR examination of some N-thioaroylmorpholine–bromine adducts
13C NMR examination of some N-thioaroylmorpholine–bromine adducts
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4′-α-C-Branched N,O-nucleosides: synthesis and biological properties
4′-α-C-Branched N,O-nucleosides: synthesis and biological properties
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Synthesis and biological evaluation of phosphonated carbocyclic 2′-oxa-3′-aza-nucleosides
Synthesis and biological evaluation of phosphonated carbocyclic 2′-oxa-3′-aza-nucleosides
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Enantioselective synthesis of homocarbocyclic-2′-oxo-3′-azanucleosides
Enantioselective synthesis of homocarbocyclic-2′-oxo-3′-azanucleosides
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Stereoselective synthesis of homochiral annulated sultams via intramolecular cycloaddition reactions
Stereoselective synthesis of homochiral annulated sultams via intramolecular cycloaddition reactions
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Stereoselective synthesis of fused γ-lactams by intramolecular nitrone cycloaddition
Stereoselective synthesis of fused γ-lactams by intramolecular nitrone cycloaddition
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Ring-opening of isoxazolidine system: Homologation of 3-aryl into 3-styryl nitrones via intermediate 5-hydroxy-isoxazolidines
Ring-opening of isoxazolidine system: Homologation of 3-aryl into 3-styryl nitrones via intermediate 5-hydroxy-isoxazolidines
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Stereoselective control in 1,3-dipolar cycloaddition of nitrones to substituted styrenes
Stereoselective control in 1,3-dipolar cycloaddition of nitrones to substituted styrenes
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Isoxazolidine analogues of pseudouridine: a new class of modified nucleosides
Isoxazolidine analogues of pseudouridine: a new class of modified nucleosides
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Stereoselective synthesis of isoxazole and pyrazole annulated sultams via intramolecular 1,3-dipolar cycloaddition reactions
Stereoselective synthesis of isoxazole and pyrazole annulated sultams via intramolecular 1,3-dipolar cycloaddition reactions
212 views