Ph <sub>2</sub> SCCO: A New Versatile CCO‐Fragment Transfer Reagent

ketenylidene (C<sub>2</sub>O) is an electronically intriguing small molecule with significant potential as a C<sub>2</sub> synthon in organic synthesis. However, its high reactivity has thus far precluded practical applications. Herein, we report the synthesis of a new reagent, the heterocumulene Ph<sub>2</sub>S═C═C═O (1), a well-defined C<sub>2</sub>O equivalent that accurately replicates the chemical reactivity profile of C<sub>2</sub>O in a controlled manner. 1 uniquely integrates ketene-like and classical carbene reactivity. In the presence of Brønsted acids, 1 undergoes initial 1,2-addition to form a sulfur ylide intermediate, which can be exploited for subsequent reactions including cyclopropanation, epoxidation, or X-H addition. The CCO fragment transfer strategy, starting from simple precursors, enables efficient access to α-cyclopropyl- as well as α-epoxy-carbonyl derivatives and structurally complex bicyclic cyclopropanes.

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Publication Details

Journal
Angewandte Chemie International Edition
Published
2025-10-10
DOI
https://doi.org/10.1002/anie.202518689
Citations
2
Primary Topic
Cyclopropane Reaction Mechanisms
Type
article
Field-Weighted Citation Impact
1.87

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article

Ph 2 SCCO: A New Versatile CCO‐Fragment Transfer Reagent

Qiu Sun, Richard Goddard, David Tymann, Max Martin Hansmann et al.
2 citations
Angewandte Chemie International Edition
Cyclopropane Reaction Mechanisms
1.87
article

Ph 2 SCCO: A New Versatile CCO‐Fragment Transfer Reagent

Qiu Sun, Richard Goddard, David Tymann, Max Martin Hansmann, Patrick W. Antoni, Julian Hauda
article en
2 citations

Abstract

ketenylidene (C<sub>2</sub>O) is an electronically intriguing small molecule with significant potential as a C<sub>2</sub> synthon in organic synthesis. However, its high reactivity has thus far precluded practical applications. Herein, we report the synthesis of a new reagent, the heterocumulene Ph<sub>2</sub>S═C═C═O (1), a well-defined C<sub>2</sub>O equivalent that accurately replicates the chemical reactivity profile of C<sub>2</sub>O in a controlled manner. 1 uniquely integrates ketene-like and classical carbene reactivity. In the presence of Brønsted acids, 1 undergoes initial 1,2-addition to form a sulfur ylide intermediate, which can be exploited for subsequent reactions including cyclopropanation, epoxidation, or X-H addition. The CCO fragment transfer strategy, starting from simple precursors, enables efficient access to α-cyclopropyl- as well as α-epoxy-carbonyl derivatives and structurally complex bicyclic cyclopropanes.

Angewandte Chemie International EditionVol. 64(47)
Max Planck Society (DE), TU Dortmund University (DE), Soochow University (CN), Max-Planck-Institut für Kohlenforschung (DE), Zero to Three (US)
Deutsche Forschungsgemeinschaft
Openalex Percentile: Top 13%
Cyclopropane Reaction Mechanisms
1.87
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