No description available.

Tübingen, Univ., Diss., 2008.

Zugl.: Stuttgart, Univ., Diss., 2010

Universiẗat, Diss., 2001--München.

No description available.

No description available.

Aziridines, three membered heterocycles containing a nitrogen in the ring, are extremely valuable to synthetic organic chemistry, as subjecting these compounds to ring opening processes initiates further capabilities for the molecule. Additionally, aziridines themselves possess the capacity and characteristics suitable for pharmaceutical applications, increasing the interest and appeal for their synthesis. One of the approaches to the formation of these products is the aza-Darzens reaction between imines and brominated nucleophiles. The research presented here aims to analyze this technique, specifically between tert-butanesulfinimines and methyl (E)-4-bromo-3-methylbut-2-enoate. Within the context of the reaction mechanism, the pivotal step involves nitrogen on a sulfinimine enolate bonding to the gamma carbon of the nucleophile, effectively cleaving bromine and producing an aziridine. Investigation into the development of the aforementioned imines and nucleophile is also accomplished in this undertaking.

The reactions of 4,6-dinitrobenzofuroxan, (DNBF) with aniline and six of its N- and ring- substituted derivatives have been studied. It is known that aniline usually reacts as a nitrogen nucleophile, forming nitrogen-bonded σ-adducts with trinitrobenzene, (TNB) in the presence of a strong base. However, in acidic solutions, a-adducts are formed with bonding between a ring carbon atom of the anilines and the 7-position of DNBF. A value of 2.0 for k(_H)/k(_D), the kinetic isotope effect, indicates that bond formation is largely rate determining in the substitution pathway. Estimates were made for the pK(_a) values relating to carbon protonation of the anilines. In solutions of aniline buffered with aniline hydrogen chloride it was possible to distinguish an initial, rapid reaction via the nitrogen centre to give anionic a-adducts. The thermodynamically more stable carbon-bonded σ-adducts were observed to form over time. In the presence of excess amine, these zwitterionic σ-adducts were in rapid equilibrium with the deprotonated forms. Equilibrium constants for this acid-base process were measured, and indicate that the negatively charged DNBF moiety is electron withdrawing relative to hydrogen. Kinetic and equilibrium studies are reported for the reactions of several aliphatic amines with a selection of nitrobenzofurazan derivatives in DMSO. Rapid reaction at the 5- position to yield σ-adducts was followed by slower formation of the thermodynamically more stable adducts at the 7-position. Proton transfer from the zwitterionic intermediates to a second molecule of amine was generally rapid, and the attack of the amine rate determining. This is in direct contrast with reactions involving TNB, where the proton transfer step is usually rate limiting. The reactions of four nitrobenzofurazan derivatives with sulfite have been studied in aqueous solutions. The stability of the initially formed 5-adducts was remarkably high in comparison with the corresponding σ-adducts formed from attack of sulfite on TNB. A slow isomerisation was observed to yield the thermodynamically more stable 7-adducts, except in the reaction with 4-nitro-7-chlorobenzofurazan, where attack at the 7-position would lead to nucleophilic substitution of the chloro-group to yield the substitution product. The mechanism of the isomerisation was found to occur via an intermolecular rearrangement, and not according to an intramolecular Boulton-Katritzky rearrangement. Sulfite attack on DNBF was also studied. A value for the equilibrium constant for the formation of a 1:1 adduct, K(_7) 1.1 x 10(^13) dm(^3) mol(^-1) was determined. This high value is a reflection of the high carbon basicity of the sulfite ion, and the highly electrophilic character of DNBF. Evidence was also obtained for the formation of 1:2 di-adducts in the presence of excess sulfite, which are present in the isomeric cis and trans forms.

Expanding the uses of the NCAL and finding the spectrum of substrates best suited for such a transformation has been the main effort of my research. Previous studies had focused on aldedydes as the requisite functionality that would provide the needed electrophilicity in order to complete the aldol; however, recent advancements have introduced ketones as a viable carbonyl. With an established protocol in hand, I set out to explore various substrates that could yield Beta-lactones in good to moderate yields such as amino acid derivatives, diones, and large cyclic formations as well as simple, straight chain acids with varying groups Alpha to the ketone. In general, I was able to establish a basic framework of substrates that are highly and/or moderately susceptible towards the NCAL and current studies continue to further expand the scope. In addition to making Beta-lactones, I investigated alkyl cuprates as soft nucleophiles to afford addition at the Beta carbon yielding a variety of acids. Substrates for cuprate additions have been expanded to bulkier and multi-cyclic Beta-lactones and applied to the synthesis of a Merck IND intermediate. Additions to bi- and tri-chloro Beta-lactones due to the presence of the resulting moity in natural products are currently being studied.

Chemnitz, Techn. Univ., Diss., 2009.