Synthesis and metal complexes of C2 symmetric ligands obtained from (R)-(+)-Betti and dialdehydes for asymmetric induction reactions


Autoria(s): Rigotti, Thomas
Contribuinte(s)

Paolucci, Claudio

Righi, Paolo

Data(s)

16/10/2015

31/12/1969

Resumo

The aim of this master’s research thesis was the employment of an enantiopure 1,3-aminoalcohol, the 1-(α-aminobenzyl)-2-naphthol, known as Betti base, for the synthesis of some novel compounds which show a C2 symmetry. Some of these compounds, after derivatization, were used as ligands in association with transition metals to prepare some catalysts for enantioselective catalytic reactions. Some aminoalcohol (Salan-type) derivatives of these compounds were obtained upon reduction and in some cases it was possible to obtain complexes with transition metals such as Mn, Ni, Co and Cu. Furthermore a novel 6-membered analogue bisoxazoline ligand, 2,6-bis((R)-1-Phenyl-1H-naphtho[1,2-e][1,3]oxazin-3-yl)pyridine, was obtained and from it two Cu-complexes were prepared. The metal complexes were employed in some reactions to test the asymmetric induction, which was in some cases up to discrete values.

Formato

application/pdf

Identificador

http://amslaurea.unibo.it/9335/1/Rigotti_Thomas_tesi.pdf

Rigotti, Thomas (2015) Synthesis and metal complexes of C2 symmetric ligands obtained from (R)-(+)-Betti and dialdehydes for asymmetric induction reactions. [Laurea magistrale], Università di Bologna, Corso di Studio in Chimica industriale [LM-DM270] <http://amslaurea.unibo.it/view/cds/CDS0884/>

Relação

http://amslaurea.unibo.it/9335/

Direitos

info:eu-repo/semantics/openAccess

Palavras-Chave #enantioselective synthesis metal complexes Betti asymmetric reactions #Chimica industriale [LM-DM270] #cds :: 0884 :: Chimica industriale [LM-DM270] #sessione :: seconda
Tipo

PeerReviewed

info:eu-repo/semantics/masterThesis

Idioma(s)

en

Publicador

Alma Mater Studiorum - Università di Bologna