Photo-induced decarboxylative C-S bond formation to access sterically hindered unsymmetric S-alkyl thiosulfonates and SS-alkyl thiosulfonates
Due to the high reactivity and versatility of benzenesulfonothioates, significant advancements have been made in constructing C-S bonds. However, there are certain limitations in the synthesis of S-thiosulfonates and SS-thiosulfonates, especially when dealing with substantial steric hindrance, which poses a significant challenge. Herein, we present an innovative approach for assembling unsymmetric S-thiosulfonates and unsymmetric SS-thiosulfonates through the integration of dual copper/photoredox catalysis. Moreover, we also realized the one-pot strategy by directly using carboxylic acids as raw materials by in-situ activation of them to access S-thiosulfonates and SS-thiosulfonates without further purification and presynthesis of NHPI esters. The envisaged synthesis and utilization of these reagents are poised to pioneer an innovative pathway for fabricating a versatile spectrum of mono-, di-, and polysulfide compounds. Furthermore, they introduce a class of potent sulfenylating reagents, empowering the synthesis of intricate unsymmetrical disulfides that were previously challenging to access.
Authors
- Guotao Lin
- Qiuling Song (ORCID: https://orcid.org/0000-0002-9836-8860)
- Jian Xu (ORCID: https://orcid.org/0009-0005-6798-8433)
- Yu Guo (ORCID: https://orcid.org/0000-0003-4952-8431)
- Mengjie Zhang (ORCID: https://orcid.org/0000-0002-8053-092X)
Institutions
- Huaqiao University (CN)
- Henan Normal University (CN)
- Fuzhou University (CN)
Publication Details
- Journal
- Nature Communications
- Published
- 2024-08-25
- DOI
- https://doi.org/10.1038/s41467-024-51334-5
- Citations
- 26
- Primary Topic
- Sulfur-Based Synthesis Techniques
- Type
- article
- Field-Weighted Citation Impact
- 6.50
Funders
- Henan Normal University
- National Natural Science Foundation of China
- Natural Science Foundation of Fujian Province
- Huaqiao University