One-pot synthesis of azepine spiro[4.6]-γ-lactams by a Hantzsch-type reaction
A facile route to spiro-γ-lactams containing fused seven- and five-membered rings is showcased here in a multicomponent reaction harnessing glycine. Four spiro-γ-lactams were characterised, including by X-ray diffraction techniques, showing them to be trapped unstable intermediates of the Strecker degradation. This hitherto unknown reaction pathway was investigated with mass spectrometry, revealing a plausible reaction mechanism.
Authors
- Scarlet L. Hopkins (ORCID: https://orcid.org/0000-0002-7015-4019)
- Jack K. Clegg (ORCID: https://orcid.org/0000-0002-7140-5596)
- Kristen T. Clarke
- William J. Gee (ORCID: https://orcid.org/0000-0002-6520-6216)
Institutions
- Griffith University (AU)
- The University of Queensland (AU)
Publication Details
- Journal
- Organic & Biomolecular Chemistry
- Published
- 2024-11-28
- DOI
- https://doi.org/10.1039/d4ob01719f
- Citations
- 1
- Primary Topic
- Chemical synthesis and alkaloids
- Type
- article
- Field-Weighted Citation Impact
- 0.25