- Docente: Stefano Masiero
- Credits: 8
- SSD: CHIM/06
- Language: Italian
- Teaching Mode: Traditional lectures
- Campus: Bologna
- Corso: Single cycle degree programme (LMCU) in Pharmaceutical Chemistry and Technology (cod. 5986)
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from Oct 02, 2024 to Jan 16, 2025
Learning outcomes
The aim of the course is to widen and deepen the knowledge of organic chemistry. The main C-C forming reactions will be presented and synthetic strategies will be discussed. The chemical properties of several classes of organic compounds, mostly of natural origin, will
be presented, together with synthetic approaches leading to them.
The student will acquire a deeper understanding of physical and chemical properties of organic compounds, which will allow an analytical approach to problem-solving and autonomous study in the field of organic chemistry.
Course contents
- Heterocyclic aromatic compounds: pyrrole, furan, thiophene, pyridine and their derivatives: structure and reactivity.
- Nucleosides, nucleotides and nucleic acids.
- Free radicals and radical reactions.
- Stereochemistry: isomers classification, stereoisomers classifications, chirality: centre, axis, plane, helix, determination of enantiomeric excess and optical purity, basics of resolution techniques and asymmetric synthesis.
- Sugars: monosaccharides, disaccharides, polysaccharides: structure and reactivity.
- Aminoacids, peptides and proteins.
- Working out organic structures: C-C bond forming reactions, enolate chemistry, protecting groups, synthetic equivalents, retrosynthetic analysis.
- Exercises on retrosynthetic analysis and synthesis planning.
- Brief overview of the main synthetic approaches to the preparation of amino acids and peptides.
Readings/Bibliography
Heterocyles
- Morrison, Boyd, Chimica organica, CEA, 1976 or subsequent.
- Hendrickson, Cram, Hammond, Chimica organica, Piccin 1973 or subsequent.
- D.T. Davies, Aromatic Heterocyclic Chemistry, Oxford University press, 1992.
- D. Sica, F. Zollo, Chimica dei composti eterociclici, Edises, 2001.
Stereochemistry
- B. Testa, Principles of organic stereochemisry, M. Dekker ed, 1979.
- E.L. Eliel, S.H. Wilen, Stereochemistry of organic compounds, Wiley ed., 1994.
Sugars
- Morrison, Boyd, Chimica organica, CEA, 1976 or subsequent.
Aminoacids and peptides
- W.H. Brown, Chimica organica, EdiSes, 1996 or subsequent.
- J. Jones, Amino acid and peptide synthesis, Oxford University Press, 1992.
- M. Bodanszki, Principles of peptide synthesis, 2nd ed. Springer, 1993.
Free radicals
- R.O.C. Norman, Chimica organica, Piccin, 1982 or subsequent.
Protecting groups
- Carey, Sundberg, Advanced organic chemistry, IV ed. or subsequent, Plenum Press.
Organic synthesis and C-C bond formation
- Carey, Sundberg, Advanced organic chemistry, IV ed. or subsequent, Plenum Press.
- March, Advanced organic chemistry, IV ed. or subsequent, Wiley.
- S. Warren, Organic Synthesis: The Disconnection Approach, Wiley, 1982 or subsequent.
- Willis, Willis, Organic synthesis, Oxford University Press, 1995.
- C. Trombini, The Construction of Molecular Architectures - Guidelines to Organic Synthesis Design, Bologna University Press, 2021, ISBN online 9788869237287
Teaching methods
Lectures
Assessment methods
In the absence of restrictions imposed by specific collective emergencies, the final examination, aiming at ascertaining the student's acquired skills, will consist of both a written and an oral test. The written test is the main one, where students will be presented with 3 questions, pertaining the course topics, which must be answered in 2 hours time (books, notes etc. are not allowed). A maximum of 10 points will be given for each question. Students ranking above 17/30 will take the oral. The oral test (45 min ca.) is meant for a more precise evaluation of the candidate and it will have the written test as the starting point. Enrolment via AlmaEsami.
Teaching tools
Presentations. Files will be made available for download
Office hours
See the website of Stefano Masiero