Repositori URV

Identificador: TDX:1321

Handle: https://hdl.handle.net/20.500.11797/TDX1321

Autors:
Liu, Chunhui

Resum:
For a long time, homogeneous catalysis was almost synonymous with transition metal catalysis, with a small niche reserved to biocatalysis. Things have changed very much in recent years. Since about the year 2000, organocatalysis, where the catalyst is a small organic molecule, often with chiral properties, has grown rapidly to become one of the most important fields in organic chemistry. As the research field is expanding its role, mechanistic knowledge becomes more critical to understand the reaction modes and as¬sist in the development of more efficient processes. Theoretical chemistry, with its abil¬ity to locate intermediates and transition states, can be very helpful in this concern. This thesis is devoted to the computational study of the mechanism of three representative organocatalytic reactions. 1. Asymmetric Friedel-Crafts hydroxyalkylation of indoles catalyzed by chiral Brønsted-acids Chiral Brønsted¬acid catalysis is a rapidly growing area of organocatalysis. Water is one of the simplest molecules with Brønsted–acid capabilities. The coordination of water molecules to the carbonyl function in Diels–Alder reactions and Claisen rearrangements results in the enhancement of the reaction rate. Carmona and co¬workers used a water molecule attached to a chiral iridium fragment as a Brønsted–acid catalyst to yield the Friedel–Crafts (FC) reaction between ethyl 3,3,3 trifluoromethylpyruvate and indole at the low temperature. Based on their experimental results, we have carried out a computational study on the mechanism of this reaction and evaluated the catalytic role of the metal complex and water in this reaction. The mechanism of this reaction is stepwise, the first step is the formation of a C¬C bond together with the transfer of a proton from water molecule