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Showing 1 to 5 of 5 for “"1,2-Amino alcohols"”.

  1. Synthesis and troubleshooting of chiral 1,2-amino alcohols leading to highly substituted bisoxazoline ligands

    Submission original under an indefinite embargo labeled 'Open Access'. The submission was exported from vireo on 2022-11-15 without embargo terms

    uiuc Repository record for Synthesis and troubleshooting of chiral 1,2-amino alcohols leading to highly substituted bisoxazoline ligands (opens in a new tab)

  2. Copper-catalyzed arylation of 1,2-amino alcohols. Synthesis of N-terminal, peptide helix initiators, and characterization of highly helical, capped polyalanine peptides

    … Ullmann reaction for N- or O-arylation of 1,2-aminoalcohols with aryl iodides is described. The procedures enjoy several advantages over traditional methods: a substoichiometric amount of copper catalyst is employed, the reactions take place in low boiling and non-toxic solvents such as …

    mit Repository record for Copper-catalyzed arylation of 1,2-amino alcohols. Synthesis of N-terminal, peptide helix initiators, and characterization of highly helical, capped polyalanine peptides (opens in a new tab)

  3. Stereoselective synthesis of 1,2-disubstitued βeta-amino alcohols and amino thiols

    … rapid construction of diverse libraries of 1,2-amino alcohols. A number of methods are examined prior to the identification of 1,2-conjugate addition of aryl and alkyl lithium reagents to Ellman sulfonimines. The use of lithium reagents is key to overcome modest diastereoselectivity and poor …

    uiuc Repository record for Stereoselective synthesis of 1,2-disubstitued βeta-amino alcohols and amino thiols (opens in a new tab)

  4. NATURAL PRODUCT INSPIRED METHODOLOGIES: ADVANCES IN DIASTEREOSELECTIVE N-SULFINYL IMINE AND TRIFLUOROPYRUVIC ACID REACTIONS

    … A one-pot protocol was developed to access 1,2 amino alcohols with high diastereoselectivity. With a good understanding of the diastereoselective reaction with NSMD and NSMEs, I joined with Dr. Po-Cheng Yu to develop a highly diastereoselective domino Michael/Michael/Mannich reaction for the …

    temple Repository record for NATURAL PRODUCT INSPIRED METHODOLOGIES: ADVANCES IN DIASTEREOSELECTIVE N-SULFINYL IMINE AND TRIFLUOROPYRUVIC ACID REACTIONS (opens in a new tab)