Strain-Releasing Hydrogenation of Donor–Acceptor Cyclopropanes and Cyclobutanes via Electrochemical Site Selective Carbonyl Reduction

An acid or hydrogen gas-free electrochemical protocol is established for the hydrogenation of strained rings (cyclopropane and cyclobutane) at room temperature and atmospheric pressure. The mechanistic study revealed that the reaction was initiated via the reduction of the carbonyl group. The methodology is highly specific toward strained rings such as cyclopropane and cyclobutane, which exhibit broad functional group tolerance.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-04-21
DOI
https://doi.org/10.1021/acs.joc.5c00180
Citations
2
Primary Topic
Cyclopropane Reaction Mechanisms
Type
article
Field-Weighted Citation Impact
1.87

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article

Strain-Releasing Hydrogenation of Donor–Acceptor Cyclopropanes and Cyclobutanes via Electrochemical Site Selective Carbonyl Reduction

Nakshatra Banerjee, Prabal Banerjee, Rakesh Kumar, Biswadeep Manna
2 citations
The Journal of Organic Chemistry
Cyclopropane Reaction Mechanisms
1.87
article

Strain-Releasing Hydrogenation of Donor–Acceptor Cyclopropanes and Cyclobutanes via Electrochemical Site Selective Carbonyl Reduction

Nakshatra Banerjee, Prabal Banerjee, Rakesh Kumar, Biswadeep Manna
article en
2 citations

Abstract

An acid or hydrogen gas-free electrochemical protocol is established for the hydrogenation of strained rings (cyclopropane and cyclobutane) at room temperature and atmospheric pressure. The mechanistic study revealed that the reaction was initiated via the reduction of the carbonyl group. The methodology is highly specific toward strained rings such as cyclopropane and cyclobutane, which exhibit broad functional group tolerance.

The Journal of Organic ChemistryVol. 90(17)
Indian Institute of Technology Ropar (IN)
Indian Institute of Technology Ropar, Science and Engineering Research Board
Openalex Percentile: Top 16%
Cyclopropane Reaction Mechanisms
1.87
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