Alkoxylation and Phosphorylation of Pyrimidine Disulfides: Green Synthesis of Alkoxypyrimidine Thioethers and Pyrimidine Phosphorothioates
This paper addresses a novel, green, and sustainable method to construct new C-S and P-S bonds by cleaving the S-S bond in pyrimidine disulfide under various conditions. The first alkoxylation and phosphorylation of pyrimidine disulfide are effectively accomplished by this approach. Compared to the methods reported, this approach provides more benefits, including the utilization of eco-friendly solvents, straightforward procedure, mild reaction conditions, high atomic efficiency, and a broad range of applicable substrates. As a result, we were able to synthesize a variety of pyrimidine phosphorothioate lipids with potential applications. Furthermore, a series of control experiments as well as theoretical calculations are performed in this work to produce deeper insights of the transfer mechanism.
Authors
- Xi‐Cun Wang (ORCID: https://orcid.org/0000-0003-3770-9817)
- Shun‐Xi Li
- Fan Gao
- Ming Li (ORCID: https://orcid.org/0000-0002-2207-0873)
- Yang Zhang (ORCID: https://orcid.org/0000-0003-4521-9228)
- Dong‐Ping Chen (ORCID: https://orcid.org/0000-0002-3103-5308)
- Wen Ma
- Chunhong Yang (ORCID: https://orcid.org/0000-0003-1087-8135)
- Zheng‐Jun Quan (ORCID: https://orcid.org/0000-0002-4393-3594)
- Zhao‐Zhen Zhou
Institutions
- Northwest Normal University (CN)
Publication Details
- Journal
- The Journal of Organic Chemistry
- Published
- 2025-02-04
- DOI
- https://doi.org/10.1021/acs.joc.4c02917
- Primary Topic
- Synthesis and Reactivity of Sulfur-Containing Compounds
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Northwest Normal University
- National Natural Science Foundation of China
- Natural Science Foundation of Gansu Province