Selective Synthesis of Mono- and Bis-Phosphorylated (Dihydro)pyrans via TMSCl-Mediated Cascade Phosphorylation Cycloisomerization of Enynones
A chlorotrimethylsilane (TMSCl)-mediated cascade phosphorylation and cycloisomerization of enynones with diphenylphosphine oxides is presented. This methodology enables the highly selective synthesis of monophosphorylated 2<i>H</i>-pyrans and bisphosphorylated dihydropyrans through precise solvent-reagent stoichiometry control. The strategy demonstrated excellent functional group compatibility and high yields (up to 96%), providing facile access to structurally diverse phosphorylated heterocycles with potential applications in medicinal chemistry and materials science.
Authors
- Xi‐Cun Wang (ORCID: https://orcid.org/0000-0003-3770-9817)
- Yi‐Feng Qiu (ORCID: https://orcid.org/0000-0002-2747-9598)
- Jian-He Cao
- Ming Li (ORCID: https://orcid.org/0000-0002-2207-0873)
- Qiang Wang (ORCID: https://orcid.org/0000-0001-9250-3067)
- Zheng‐Jun Quan (ORCID: https://orcid.org/0000-0002-4393-3594)
- Dong-Qian Xue
- Yong‐Min Liang (ORCID: https://orcid.org/0000-0001-8280-8211)
Institutions
- Northwest Normal University (CN)
- Lanzhou University (CN)
Publication Details
- Journal
- Organic Letters
- Published
- 2024-09-26
- DOI
- https://doi.org/10.1021/acs.orglett.4c03397
- Citations
- 7
- Primary Topic
- Asymmetric Synthesis and Catalysis
- Type
- article
- Field-Weighted Citation Impact
- 1.75
Funders
- Northwest Normal University
- National Natural Science Foundation of China