Sintesi di molecole organiche enantiomericamente arricchite con l'uso della catalisi organica

The main topic of this thesis is the use of organocatalysis to synthesize organic compounds enantiomerically enriched. The first matter is about the synthesis of α-amino thioester derivatives through a tandem condensation-intramolecular rearrangement-protonation, this is a conceptually novel chiral Brønsted base/ Brønsted acid catalytic method that provides a number of important synthetic building blocks in good yields and with moderate and good enantioselectivities. The second topic is concerned to the synthesis of aldols derivatives of pyridine carbaldehydes functionalized in different positions using simple amino acids derivatives as catalysts, for example L-proline, L-pyrrolidine tetrazole and so on. This is important because is necessary to found news synthetic methods to produce pyridines nucleus that are very important building block for drugs. Following it is illustrated a preliminary result of a new methodological approach to the synthesis of enantiomerically enriched cyclopentanones starting from cyclobutanones and spirocyclopentanones, it is possible to expand the ring through an organocatalysed Michael reaction. This new approach takes advantages of the introduction of the α,β-unsatured aldehyde function on cyclobutanones. Finally, supramolecular interactions by halogen bonding are described. These occurs between enatiomerically enriched aldols benzothiophene derivatives, synthesized by means of organocatalysed reactions. These kinds of interactions are strongly important in supramolecular chemistry but also in biochemistry, materials and crystal engineering.

Grantor dc:publisher

Università degli Studi di Cagliari

Year dc:date

2014

Author dc:creator

• PITZANTI, PATRIZIA

• asymmetric organocatalysis
• benzotiophene derivatives
• composti spiranici
• derivati benzotiofenici
• derivati di α-amminoacidi
• organo catalisi asimmetrica
• piridine carbaldeidi
• pyridine carbaldehydes
• spiro-compounds
• α-aminoacids derivatives
• Settore CHIM/06 - Chimica Organica

Statement dc:rights

• info:eu-repo/semantics/openAccess
• license:Non specificato

Language dc:language

ita

Handle dc:identifier

http://hdl.handle.net/11584/266431

OAI identifier oai:identifier

oai:iris.unica.it:11584/266431