Carlo Siciliano
0000-0002-0584-219X
53 papers found
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A preparation of N-Fmoc-N-methyl-α-amino acids and N-nosyl-N-methyl-α-amino acids
Extraction of Quinolizidine Alkaloids in Non Aqueous Basic Conditions: The Case of Spartium junceum Flowers
Comparison of the Volatile Constituents in Cold-Pressed Bergamot Oil and a Volatile Oil Isolated by Vacuum Distillation
D-homoannulation of 17α,21-dihydroxy-20-keto steroids (corticosteroids)
Optically PureN-Hydroxy-O-triisopropylsilyl-α-l-amino Acid Methyl Esters from AlCl3-Assisted Ring Opening of Chiral Oxaziridines by Nitrogen Containing Nucleophiles
A Convenient Method for the Stereoselective Conversion of Aryl Peptidyl Ketones into the Corresponding Aryl Aminomethin Derivatives, A Novel Class of Modified Peptides
Determination by gas chromatography/mass spectrometry of p-phenylenediamine in hair dyes after conversion to an imine derivative
Alternative and Chemoselective Deprotection of the ?-Amino and Carboxy Functions ofN-Fmoc-Amino Acid andN-Fmoc-Dipeptide Methyl Esters by Modulation of the Molar Ratio in the AlCl3/N,N-Dimethylaniline Reagent System
Binding Mode of TMC-95A Analogues to Eukaryotic 20S Proteasome
SPE?GC?MS Analysis of Chloroform in Drinking Water
An efficient and highly selective deprotection of N-Fmoc-alpha-amino acid and lipophilic N-Fmoc-dipeptide methyl esters with aluminium trichloride and N,N-dimethylaniline
Quantitative analysis of human salivary glucose by gas chromatography–mass spectrometry
Highly Stereoselective Conversion of Aryl Peptidyl Ketones into the Corresponding Peptide Alcohols.
TMC-95A Analogues with Endocyclic Biphenyl Ether Group as Proteasome Inhibitors
Highly Stereoselective Synthesis of Optically Pure C-Aryl Imines from α-L-Amino Acid Methyl Esters.
Reactivity Models of 1-N-Vinyluracil and Synthesis of a New Class of Potential Antiviral Agents by the Use of 1,3-Dipolar Cycloaddition Reactions
Synthesis of a TMC-95A Ketomethylene Analogue by Cyclization via Intramolecular Suzuki Coupling
A straightforward chemical synthesis of 17-ketosteroids by cleavage of the C-17-dihydroxy acetone side chain in corticosteroids
A facile approach to steroidal 20-hydroxy-17(20)-en-21-aldehydes: important intermediates in the biological 17-dehydroxylation of C-17 dihydroxyacetone steroids
Facile Approach to Enantiomerically Pure α-Amino Ketones by Friedel−Crafts Aminoacylation and Their Conversion into Peptidyl Ketones
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