Recent Advancements in Metal‐Free Catalysis for Cyclopropane Ring Cleavage

Abstract Over the last decade, there have been notable advances in the field of ring opening reaction of numerous cyclopropane derivatives under metal‐free conditions including donor–acceptor cyclopropanes, acceptor‐activated cyclopropanes, alkylidenecyclopropanes, cyclopropyl alcohols, and vinylidenecyclopropanes. This review article aims to offer a comprehensive overview on cleavage reactions of cyclopropanes using Bronsted and Lewis acids, organic and inorganic bases, TCT‐DMF, ionic liquids etc. Photoinduced and catalyst‐free ring cleavage of cyclopropanes are also accentuated in this review.

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Publication Details

Journal
ChemistrySelect
Published
2025-03-01
DOI
https://doi.org/10.1002/slct.202500035
Citations
5
Primary Topic
Cyclopropane Reaction Mechanisms
Type
article
Field-Weighted Citation Impact
4.68
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article

Recent Advancements in Metal‐Free Catalysis for Cyclopropane Ring Cleavage

Amit Pramanik, Sanjay Bhar, Asit Kumar Das, Avishek Ghatak
5 citations
ChemistrySelect
Cyclopropane Reaction Mechanisms
4.68
article

Recent Advancements in Metal‐Free Catalysis for Cyclopropane Ring Cleavage

Amit Pramanik, Sanjay Bhar, Asit Kumar Das, Avishek Ghatak
article en
5 citations

Abstract

Abstract Over the last decade, there have been notable advances in the field of ring opening reaction of numerous cyclopropane derivatives under metal‐free conditions including donor–acceptor cyclopropanes, acceptor‐activated cyclopropanes, alkylidenecyclopropanes, cyclopropyl alcohols, and vinylidenecyclopropanes. This review article aims to offer a comprehensive overview on cleavage reactions of cyclopropanes using Bronsted and Lewis acids, organic and inorganic bases, TCT‐DMF, ionic liquids etc. Photoinduced and catalyst‐free ring cleavage of cyclopropanes are also accentuated in this review.

ChemistrySelectVol. 10(9)
Jadavpur University (IN), Murshidabad Medical College and Hospital (IN)
Openalex Percentile: Top 6%
Cyclopropane Reaction Mechanisms
4.68
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