LEARNING OUTCOMES

Further insight into the reactivity of organic molecules through the study of difunctional molecules. Carbon-carbon bond forming reactions with particular emphasis on the costruction of cyclic systems. Heterocycles. Natural organic substances.

TEACHING METHODS

The lessons are given in the traditional way (64 hours in the classroom). The attendance is highly recommende.

If necessary lessons will be given on-line through an appropriate platform.

SYLLABUS/CONTENT

1.     FURTHER INSIGHT INTO THE REACTIVITY AND PREPARATION OF BIFUNCTIONAL COMPOUNDS (24 hours, Prof. Banfi)

• A1 Polyunsaturated and polycyclic systems and bicarboxylic compounds
  • A1.1 Conformations of cycloalkanes and bicycloalkanes
    • A1.1.2 Conformation of fused bicyclic alkanes
    • A1.1.1 Conformations of monocyclic alkanes
    • A1.1.3 Nomenclature and properties of bridged bicyclic systems
  • A1.2 Dienes
    • A1.2.1: Conjugation and UV-visible absorption
    • A1.2.2: Electrophilic addition to conjugated dienes
    • A1.2.3: Pericyclic cycloadditions: the Diels-Alder reaction
    • A1.2.4 Ring-closing metathesis
    • A1.2.5 Allenes
  • A1.3 Bicarboxylic acids
  • A1.4 Aromatic polycyclic systems
    • A1.4.1: Nomenclature and properties
    • A1.4.2: Fullerenes, graphite, graphene, carbon nanotubes
    • A1.4.3: Arene oxides
    • A1.4.4: Electrophilic substitutions on naphthalene
  • A1.5 Biaryl systems
    • A1.5.1 Chirality in biaryls
    • A1.5.2 Suzuki reaction for the synthesis of biaryls and dienes
• A2 Compounds with two oxygenated functions or one oxygenated function and an unsaturation
  • A2.1 Conjugated carbonyl and carboxylic compounds
    • A2.1.1 Preparation through: halogenation/elimination, crotonic condensation, Knoevenagel reaction; intramolecular metathesis; Wittig and Horner-Wadsworth-Emmons reactions
    • A2.1.2 Synthetic equivalence
    • A2.1.3 Conjugated nucleophilic additions: reactions with mild nucleophiles, with organometallic reagents, with hydrides, Michael reaction.
    • A2.1.4 Robinson annulation
    • A2.1.5 Conjugated additions in biology
    • A2.1.6 Conjugated additions and other reactions of enamines
  • A2.2 1,3-Dioxygenated compounds
    • A2.2.1: Cross aldol reactions with enolate preformation
    • A2.2.2: Cross alsol reactions with synthetic equivalents of aldehydes
    • A2.2.3 Oxidations with diacetoxyiodobenzene and Swern oxidation
    • A2.2.4 Claisen and Dieckmann condensations
    • A2.2.5 Aldol additions and Claisen condensations in biology
  • A2.3 1,2-Dioxygenated compounds
    • A2.3.1 Retrosynthetic strategies: logical and illogical disconnections
    • A2.3.2 Cyanide anion as acyl anion equivalent
    • A2.3.3 Isocyanides: Passerini reaction
    • A2.3.4 Dithianes
    • A2.3.5 1,2-Diols
    • A2.3.6 Cyclic acetals
• A3 Radical reactions, phenols, quinones
  • A3.1 Radical reactions
    • A3.1.1: Generality
    • A3.1.2: Radical polymerizations
    • A3.1.3 Autooxidations   
    • A3.1.4 Anti-oxidants
  • A3.2 Phenols as natural anti-oxidants
  • A3.3 Quinones

2.     HETEROCYCLIC COMPOUNDS (21 h, Prof. Riva).

• B1 Classification and nomenclature of heterocyclic compounds
• B2 Electronrich aromatic heterocycles
  • B2.1 General features
  • B2.2 Synthesis and reactivity of pyrrole, furan, thiophene and related benzo-fused compounds
• B3 Electronpoor aromatic heterocycles
  • B3.1 General features
  • B3.2 Synthesis and reactivity of pyridine, quinoline, isoquinoline, pyrimidine, pyrazine, pyridazine
• B4 Aromatic penta-atomic heterocycles with two heteroatoms
  • B4.1 General features
  • B4.2 Synthesis and reactivity of imidazole, oxazole, isoxazole
• B5 Saturated strained heterocycles: structure, synthesis and reactivity of oxiranes, aziridines, oxetanes, azetidines

3.    BIOMOLECULES (19 h, Prof. Riva).

• C1 Carbohydrates
  • C1.1 Monosaccharides
    • C1.1.1 Stereochemical families
    • C1.1.2 Fischer and Haworth formulas, pyranose and furanose conformations
    • C1.1.3 Anomeric effect
    • C1.1.4 Mutarotation
    • C1.1.5 Behavior of monosaccharides in acids and in bases
    • C1.1.6 Reduction and oxidation reactions; reducing sugar assays
    • C1.1.7 Glycosides: structure, properties and synthesis of simple glycosides
    • C1.1.8 Synthetic strategies for the synthesis of complex glycosides through chemical means (use of protecting groups and activation of glycosyl donor). Enzymatic synthesis
    • C1.1.9 Osazones
    • C1.1.10 Kiliani-Fischer synthesis
    • C1.1.11 Ruff and Wohl degradationsC1.1.12 Determination of relative and absolute configuration of main monosaccharides
  • C1.2 Disaccharides: maltose, cellobiose, saccharose and lactose
  • C1.3 Polysaccharides: structure and properties of main polysaccharides (starch, glycogen, cellulose, chitin, pectin, hyaluronic acid)
  • C1.4 Antigene determinants of cells; blood groups
  • C1.5 Glycoconjugates
    • C1.5.1 glycolipids
    • C1.5.2 glycoproteins
• C2 Lipids
  • C2.1 Fatty acids and derivatives (amides, waxes)
  • C2.2 Eicosanoides (prostaglandins etc.)
  • C2.3 Glycerolipids (triglycerides: fats, oils)
  • C2.4 Soaps and tensioactive compounds
  • C2.5 Glycerophospholipids
  • C2.6 Sphingolipids
  • C2.7 Terpenes, Terpenoids and their biosynthesis
  • C2.8 Steroids
• C3 Amino acids
  • C3.1 Nomenclature
  • C3.2 Structure and classification
  • C3.3 Acid-base properties
  • C3.4 Isoelectric point
  • C3.5 Synthesis of alpha-amino acids (from alpha-haloacids, from acylaminomalonic esters, through reducing amination, through enantioselective reduction of alpha-acylaminoacrylic acids, through Strecker reaction)
  • C3.6 Resolution of racemic alpha-amino acids
• C4 Peptides and proteins
  • C4.1 Primary structure, disulfide bonds.
  • C4.2 Protein denaturation
  • C4.3 Determination of primary structure
    • C4.3.1 Through exhaustive hydrolysis coupled with ion exchange chromatography and visualization with ninhydrin
    • C4.3.2 Through Edman method
    • C4.3.3 Through use of cyanogen bromide
    • C4.3.4 Through enzymatic methods
  • C4.4 Chemical synthesis in solution (from left to right and from right to left; use of protecting groups; activation of carboxylic function) and in solid phase (Merrifield resins)
• C5 Nucleic acids
  • C5.1 Nitrogen bases
  • C5.2 Sugars
  • C5.3 Nucleosides
  • C5.4 Nucleotides
  • C5.5 Oligonucleotides and Nucleic acids
  • C5.6 Secondary and tertiary structure of DNA
  • C5.7 Examples of genetic mutations

RECOMMENDED READING/BIBLIOGRAPHY

• Chimica Organica AA. VV. a cura di B. Botta Edi-Ermes
• Chimica Organica di M. Loudon, EdiSES
• Chimica Organica di J. McMurry, Piccin
• Chimica Organica di P. Y. Bruice, EdiSES
• Chimica Organica di P. C. Vollhardt e N. E. Schore, Zanichelli
• Chimica Organica di W. H. Brown, B. L. Iverson, E. V. Anslyn, C. S. Foote, EdiSES
• Chimica dei Composti Eterociclici di D. Sica, F. Zollo - EdiSES (l'ultima edizione)
• Chimica degli Eterocicli di G. Broggini, G. Zecchi – vol. 1 LaScientifica