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Showing result 1 - 5 of 12 swedish dissertations matching the above criteria.
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1. Reaction Between Grignard reagents and Heterocyclic N-oxides : Synthesis of Substituted Pyridines, Piperidines and Piperazines
Abstract : This thesis describes the development of new synthetic methodologies for preparation of bioactive interesting compounds, e.g. substituted pyridines, piperidines or piparazines. Thesecompounds are synthesized from commercially available, cheap and easily prepared reagents, videlicet the reaction between Grignard reagents and heterocyclic N-oxides. READ MORE
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2. New C-C coupling Reactions Enabled by Main-group Organometallics
Abstract : The carbon-carbon bond has always been at the very core of chemical research. Strategies for the creation of C−C bonds are one of the keys to the construction game that organic chemists play with the building blocks provided by Nature, with the ultimate goal of producing useful molecular structures that will serve society as medicines, materials, imaging tools, catalysts, and ligands (to mention but a few). READ MORE
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3. New Methodologies in Organic Chemistry: Applications to the Synthesis of α-Amino Acids and Natural Products
Abstract : This thesis deals with the development and application of new synthetic methodology in organic chemistry. The first part describes the development of a new protocol for the synthesis of 3-pyrrolines by means of a microwave-assisted ring-expansion reaction of 2-vinylaziridines. READ MORE
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4. Regiocontrol in copper(I)-catalyzed allylic substitution reactions with Grignard reagents : mechanistic and synthetic aspects
Abstract : .... READ MORE
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5. Iron catalyzed C-C coupling reactions - mechanistic investigations
Abstract : The mechanism of the iron catalyzed cross coupling of aryl electrophiles with alkyl Grignard reagents was studied. The reaction proceeds via a rate-limiting oxidative addition of the aryl halide to an Fe(I) complex generated in situ. A transmetalation from an aryl Grignard reagent occurs either before or after the oxidative addition. READ MORE