Synergistic Base- and Photo-Catalyzed Vicinal Trans -Selective Dideuteration of Cyclopropenes with Diarylphosphine Oxides and Potassium Glyoxylates
The development of efficient methods for trans-selective vicinal dideuteration remains an important yet challenging goal. We report a synergistic strategy that combines base-promoted H/D exchange of cyclopropenes with photoinduced radical addition, employing diarylphosphine oxides or glyoxylic acids as radical precursors and D2O as the sole deuterium source. Under mild conditions, a wide range of substituted cyclopropenes and radical precursors are well tolerated, delivering trans-dideuterated cyclopropyl phosphine oxides and carbonylated cyclopropanes in moderate to excellent yields with high deuterium incorporation.
Authors
- Tao Cao (ORCID: https://orcid.org/0000-0002-8309-5695)
- Peng Cao (ORCID: https://orcid.org/0000-0002-2044-3074)
- Yuanqing Wu
- Daoan Zhou
- Yulin Han
- Ruihao Chen
Institutions
- Nanjing University of Chinese Medicine (CN)
- Jiangsu Provincial Academy of Traditional Chinese Medicine (CN)
- Zhejiang Shuren University (CN)
Publication Details
- Journal
- The Journal of Organic Chemistry
- Published
- 2026-11-06
- DOI
- https://doi.org/10.1021/acs.joc.6c01917
- Primary Topic
- Cyclopropane Reaction Mechanisms
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Natural Science Foundation of China
- National Key Research and Development Program of China