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Showing 1 to 12 of 12 for “"Azaheterocycles"”.

  1. A Diversity-Oriented Synthesis Approach to Functionalized Azaheterocycles using Cyclic Alpha-Halo Eneformamides

    Functionalized piperidines, azepanes, azamacrocycles, morpholines, and thiomorpholines are common structural motifs found in a wide range of pharmaceuticals such as carmegliptine, levofloxacin, thioridazine, claviciptic acid, and azithomycin. As a result, there is a strong desire to construct …

    central-wash Repository record for A Diversity-Oriented Synthesis Approach to Functionalized Azaheterocycles using Cyclic Alpha-Halo Eneformamides (opens in a new tab)

  2. Total synthesis and study of myrmicarin alkaloids

    … palladium catalyzed N-vinylation of azaheterocycles with vinyl triflates is described. Cyclic and acyclic vinyl triflates along with non-nucleophilic azaheterocycles were found to be substrates for this palladium catalyzed synthesis of N-vinyl pyrrole and indole derivatives. III. …

    mit Repository record for Total synthesis and study of myrmicarin alkaloids (opens in a new tab)

  3. Methodology for the syntheses of pharmaceutically significant functional groups

    … herein: the selective benzylic fluorinations of azaheterocycles via a nitrogen-fluorine halogen bond, the synthesis of sulfoxides and sulfenamides from highly reactive and unstable chloramine in continuous-flow, and partial translation of the process route to enantiopure (S)-naproxen from batch …

    mit Repository record for Methodology for the syntheses of pharmaceutically significant functional groups (opens in a new tab)

  4. Novel metal- and main group-catalyzed methods for modulating molecular oxygenation

    … implemented to oxidize the benzylic positions of azaheterocycles. Coordination of a metal catalyst to the nitrogen lone pair is thought to induce weakening of proximal C-H bonds such that a radical catalyst with tunable chemoselectivity breaks this weakened bond. In the presence of an oxygen …

    mit Repository record for Novel metal- and main group-catalyzed methods for modulating molecular oxygenation (opens in a new tab)

  5. Development of transitional metal-catalyzed reactions for organic synthesis

    … the presence of both lactams as well as azaheterocycles in the [beta]-position of various enoates. This has led to the asymmetric synthesis of a number of interesting [5- amino acid derivatives. Chapter 4. A copper-catalyzed conjugate reduction reaction that allows for a variety of …

    mit Repository record for Development of transitional metal-catalyzed reactions for organic synthesis (opens in a new tab)

  6. Organophosphorus-Catalyzed Reductive Functionalization of Nitrocompounds via P(III)/P(V) Redox Couple

    … sequence, yielding a variety N-functionalized azaheterocycles (oxindoles, indoles, quinoxalinediones, and benzimidazoles). Besides boronic acids, anilines were also introduced as an exogenous coupling partner for novel cross-selective intermolecular N–N bond forming reactivity in the formation …

    mit Repository record for Organophosphorus-Catalyzed Reductive Functionalization of Nitrocompounds via P(III)/P(V) Redox Couple (opens in a new tab)

  7. Direct synthesis of pyridine and pyrimidine derivatives

    … and readily converted to the corresponding azaheterocycles. II. Single-Step Synthesis of Pyrimidine Derivatives. The single-step conversion of various N-vinyl and N-aryl amides to the corresponding pyrimidine and quinazoline derivatives, respectively, is described. The process involves amide …

    mit Repository record for Direct synthesis of pyridine and pyrimidine derivatives (opens in a new tab)

  8. Stereoselective monoalkyl diazene synthesis for mild reductive transformations : direct synthesis of densely substituted pyridines and pyrimidines

    … in this chemistry provides versatile azaheterocycles poised for further derivatization. The synthesis of a variety of previously inaccessible C2- and C4- pyrimidine derivatives using this methodology is noteworthy.

    mit Repository record for Stereoselective monoalkyl diazene synthesis for mild reductive transformations : direct synthesis of densely substituted pyridines and pyrimidines (opens in a new tab)

  9. Synthesis of 4-(trifluoromethyl)azetidin-2-one building blocks and their transformation into novel CF3-substituted amines and heterocyclic systems

    … diverse set of functionalized CF3-amines and CF3-azaheterocycles was investigated. In particular, 3-benzyloxy-4-trifluoromethyl-β-lactams were conveniently synthesized as a first new class of building blocks. The aptitude of these systems with respect to ring-opening reactions was explored to …

    ghent Repository record for Synthesis of 4-(trifluoromethyl)azetidin-2-one building blocks and their transformation into novel CF3-substituted amines and heterocyclic systems (opens in a new tab)