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Showing 1 to 3 of 3 for “"aziridine-ring-opening"”.

  1. Synthesis of Bicyclic and Tricyclic Analogues of Oxazolidinone

    … of ANB-22 and ANB-40. </p><p>By employing the aziridine-ring-opening and the Mitsunobu reaction, a series of fused bicyclic and tricyclic oxazolidinone-piperazine derivatives have been prepared. Using similar synthetic strategy and subsequent structural modification, the fused tricyclic …

    ohiolink Repository record for Synthesis of Bicyclic and Tricyclic Analogues of Oxazolidinone (opens in a new tab)

  2. Organocatalytic synthesis of chiral non-racemic aziridines, labelled with 2H, 15N, 13C stable isotopes

    Aziridines are ‘keystone’ synthetic building blocks - relatively reactive, three-membered heterocycles with the potential for generating ‘secondary’ high value entities such as α- or β-amino acids via ring-opening reactions. Within this thesis, a one-pot asymmetric organocatalytic methodology is …

    east-anglia Repository record for Organocatalytic synthesis of chiral non-racemic aziridines, labelled with 2H, 15N, 13C stable isotopes (opens in a new tab)

  3. Nickel precatalysts as enabling tools for catalytic coupling reactions

    … and requires no exclusion of air or water during setup. Synthesis of the precatalyst is accomplished through a straightforward procedure that employs inexpensive, commercially available reagents, requires no purification steps, and proceeds in high yield. [Chemical formula] The …

    mit Repository record for Nickel precatalysts as enabling tools for catalytic coupling reactions (opens in a new tab)