<i>meta</i> -Sulfonylation of Pyridines from Sulfur Dioxide with Dearomatized Pyridines as Redox-Active Substrates
-sulfonylation of pyridines via a dearomatization and rearomatization strategy from sulfur dioxide with thianthrenium salts as radical precursors. Mechanistic studies indicated that oxazino-pyridine substrates serve as redox-active substrates that quench the excited photocatalyst.
Authors
- Jianmin Wu (ORCID: https://orcid.org/0000-0002-0999-9194)
- Yahan Zhang
- Chunfang Huang
- Yuchan Lin
- Xinhua Wang
Institutions
- Jinggangshan University (CN)
- Chinese Academy of Sciences (CN)
- Shanghai Institute of Organic Chemistry (CN)
- ZheJiang Institute For Food and Drug Control (CN)
- State Key Laboratory of Organometallic Chemistry
- Henan Normal University (CN)
- Taizhou University (CN)
Publication Details
- Journal
- Organic Letters
- Published
- 2026-04-30
- DOI
- https://doi.org/10.1021/acs.orglett.6c01463
- Primary Topic
- Sulfur-Based Synthesis Techniques
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Henan Normal University
- National Natural Science Foundation of China
- Zhejiang Provincial Ten Thousand Plan for Young Top Talents
- Natural Science Foundation of Zhejiang Province