Ring-Enlargement of in Situ Generated Cyclopropanones with Carbonyls and Imines: Synthesis of γ-Butyrolactones and -lactams
We report a ring-enlargement of in situ generated cyclopropanones with aldehydes, ketones, and aldimines to access γ-butyrolactones and γ-lactams. Using bench-stable 1-sulfonylcyclopropanols as cyclopropanone precursors, the reaction proceeds under mild conditions and affords the products in yields of up to 84% across a range of carbonyl and imine coupling partners. Mechanistic experiments and DFT studies provide insight into the reaction pathway.
Authors
- Heinrich F. von Köller (ORCID: https://orcid.org/0009-0009-4628-7071)
- Arthur Semmelmaier (ORCID: https://orcid.org/0009-0003-8840-0315)
- Richard Herzog
- Daniel B. Werz
- Marvin Lange
Institutions
- University of Freiburg (DE)
Publication Details
- Journal
- Organic Letters
- Published
- 2026-04-01
- DOI
- https://doi.org/10.1021/acs.orglett.6c00839
- Primary Topic
- Cyclopropane Reaction Mechanisms
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Deutsche Forschungsgemeinschaft