HFIP-Promoted Bis-Phosphorylation via Dual C–P Coupling of Unprotected sec -Propargylic Alcohols and Phosphites: Access to Substituted (Prop-2-ene-1,2-diyl)( E )-Bisphosphonates
Abstract A first HFIP-promoted, direct coupling of unprotected secondary propargyl alcohols and phosphites has been developed, providing efficient access to substituted (prop-2-ene-1,2-diyl)(E)-bisphosphonates through the concurrent formation of P–C(sp2) and P–C(sp3) bonds. This transition-metal-free reaction proceeds rapidly at room temperature, featuring operational simplicity and scalability to gram quantities. Moreover, HFIP was recycled for further use by distillation, which makes this protocol a greener and more sustainable choice.
Authors
- Yufen Zhao (ORCID: https://orcid.org/0000-0003-3560-435X)
- Hua Zhao (ORCID: https://orcid.org/0000-0003-1169-6149)
- Hongbin Zhai (ORCID: https://orcid.org/0000-0003-0955-3405)
- Showkat Ahmad Bhat
- Chao Zhang
- Xi Peng
Institutions
- Ningbo University (CN)
- Xiamen University (CN)
- Peking University (CN)
Publication Details
- Journal
- The Journal of Organic Chemistry
- Published
- 2026-10-23
- DOI
- https://doi.org/10.1021/acs.joc.6c01262
- Primary Topic
- Organophosphorus compounds synthesis
- Type
- article
- Field-Weighted Citation Impact
- 0.00