A TFPN-mediated acyl fluoride platform: efficient synthesis of esters, thioesters, and macrolactones from carboxylic acids with diverse nucleophiles
A TFPN-mediated esterification strategy enables the rapid synthesis of esters, thioesters, and macrolactones via in situ acyl fluorides. This process has a broad substrate scope and excellent functional group tolerance, as well as stereoretention.
Authors
- Qiuyi Zheng
- Peng Shen (ORCID: https://orcid.org/0000-0001-6748-6111)
- Silin Xu
- Jiahui Zhang (ORCID: https://orcid.org/0000-0003-1844-7241)
- Yao Zhang (ORCID: https://orcid.org/0000-0002-6509-0946)
- Dou Zhang (ORCID: https://orcid.org/0000-0001-8555-2784)
- Jinhua Yang
- Chunyu Han
Institutions
- Hubei Normal University (CN)
- Xuchang University (CN)
Publication Details
- Journal
- Organic Chemistry Frontiers
- Published
- 2025-01-01
- DOI
- https://doi.org/10.1039/d5qo00651a
- Citations
- 4
- Primary Topic
- Sulfur-Based Synthesis Techniques
- Type
- article
- Field-Weighted Citation Impact
- 3.74