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Showing 1 to 4 of 4 for “"Hofmann rearrangement"”.

  1. The asymmetric synthesis of (2S,3R)-capreomycidine and the total synthesis of capreomycin IB

    … diaminopropanoic residue is accomplished by a Hofmann rearrangement.

    colostate Repository record for The asymmetric synthesis of (2S,3R)-capreomycidine and the total synthesis of capreomycin IB (opens in a new tab)

  2. ELECTROCHEMICAL ORGANIC TRANSFORMATIONS: FROM THE DEVELOPMENT OF ENANTIOSELECTIVE STRATEGIES TO CONTINUOUS-FLOW METHODOLOGIES

    … strategies for C(sp2)-C(sp3) bond formation, rearrangements, and C-Cl bond construction in both aliphatic and (hetero)aromatic frameworks. In the first part, the enantioselective α-chlorination of aldehydes is revisited by replacing classical chemical oxidants with anodic oxidation. Cyclic …

    milano Repository record for ELECTROCHEMICAL ORGANIC TRANSFORMATIONS: FROM THE DEVELOPMENT OF ENANTIOSELECTIVE STRATEGIES TO CONTINUOUS-FLOW METHODOLOGIES (opens in a new tab)

  3. De Novo Design of secondary structures: Synthesis and conformational studies

    … via an efficient modification of the Hofmann rearrangement. The reaction affords the desired compounds from protected asparagine or glutamine in good to high yield, using PhI(OAc)2 as source of iodine(III).

    bologna Repository record for De Novo Design of secondary structures: Synthesis and conformational studies (opens in a new tab)

  4. Design and synthesis of potential chrome-based anti-tuberculosis agents

    This dissertation describes the design and synthesis of 4-(4-oxochromen-3-yl)-3,4-dihydropyrimidin-2-one derivatives and the assessment of their biological activity against a strain of the causative agent of TB. In this investigation, two classes of chromone-based compounds were synthesised. …

    venda Repository record for Design and synthesis of potential chrome-based anti-tuberculosis agents (opens in a new tab)