-amino acid organocatalysts in the asymmetric michael addition of isobutyraldehyde to n-substituted maleimides

HIGHLIGHTS

  • who: Viktu00f3ria Kozma and collaborators from the Department of Organic Chemistry, University of Szeged, Du00f3m tu00e9r, Szeged, Hungary have published the article: -Amino Acid Organocatalysts in the Asymmetric Michael Addition of Isobutyraldehyde to N-Substituted Maleimides, in the Journal: Catalysts 2022, 992 of /2022/
  • what: The authors disclose several unexpected and interesting structural effects of aliphatic and cycloaliphatic u03b2-amino acids obtained in the enantioselective conjugate addition of isobutyraldehyde to N-benzylmaleimide. The in this study is toreactions investigate yet poorly explored. The authors focused on 2-aminocyclohexane-1-carboxylic acids bearing additional substituents on . . .

     

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