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.

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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

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article

Ring-Enlargement of in Situ Generated Cyclopropanones with Carbonyls and Imines: Synthesis of γ-Butyrolactones and -lactams

Heinrich F. von Köller, Arthur Semmelmaier, Richard Herzog, Daniel B. Werz et al.
Organic Letters
Cyclopropane Reaction Mechanisms
article

Ring-Enlargement of in Situ Generated Cyclopropanones with Carbonyls and Imines: Synthesis of γ-Butyrolactones and -lactams

Heinrich F. von Köller, Arthur Semmelmaier, Richard Herzog, Daniel B. Werz, Marvin Lange
article en

Abstract

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.

Organic LettersVol. 28(15)
University of Freiburg (DE)
Deutsche Forschungsgemeinschaft
Openalex Percentile: Top 33%
Cyclopropane Reaction Mechanisms
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