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.
Authors
- Qiu Sun (ORCID: https://orcid.org/0000-0003-3345-3391)
- Richard Goddard (ORCID: https://orcid.org/0000-0003-0357-3173)
- David Tymann
- Max Martin Hansmann (ORCID: https://orcid.org/0000-0003-3107-1445)
- Patrick W. Antoni
- Julian Hauda
Institutions
- Max Planck Society (DE)
- TU Dortmund University (DE)
- Soochow University (CN)
- Max-Planck-Institut für Kohlenforschung (DE)
- Zero to Three (US)
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
Funders
- Deutsche Forschungsgemeinschaft