DOI

Decomposition of α-diazo-γ-butyrolactams in the presence of aromatic and heteroaromatic amines, under Rh2(esp)2 catalysis, led to corresponding α-arylamino-γ-butyrolactams, which are of significant value for medicinal chemistry. The reaction scope encompasses primary as well as secondary, diversely substituted anilines and heteroaromatic amines. Insertion into the anilinic amino group was shown to be selective over amide and sulfonamide N–H insertion.

Original languageEnglish
Pages (from-to)4377-4383
Number of pages7
JournalEuropean Journal of Organic Chemistry
Volume2019
Issue number27
DOIs
StatePublished - 23 Jul 2019

    Research areas

  • Amimnes, Homogeneous catalysis, Lactams, N–H insertion, ORGANIC-SYNTHESIS, DESIGN, N-H insertion, N-H BONDS, POTENT, CARBONIC-ANHYDRASE IX, CARBENE INSERTION, INHIBITORS, SELECTIVITY

    Scopus subject areas

  • Physical and Theoretical Chemistry
  • Organic Chemistry

ID: 46204034