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.

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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
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article

One-pot synthesis of azepine spiro[4.6]-γ-lactams by a Hantzsch-type reaction

Scarlet L. Hopkins, Jack K. Clegg, Kristen T. Clarke, William J. Gee
1 citations
Organic & Biomolecular Chemistry
Chemical synthesis and alkaloids
0.25
article

One-pot synthesis of azepine spiro[4.6]-γ-lactams by a Hantzsch-type reaction

Scarlet L. Hopkins, Jack K. Clegg, Kristen T. Clarke, William J. Gee
article en
1 citations

Abstract

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.

Organic & Biomolecular ChemistryVol. 23(3)
Griffith University (AU), The University of Queensland (AU)
Openalex Percentile: Top 46%
Chemical synthesis and alkaloids
0.25
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