Photo-Induced Thiocyanation/Selenothiocyanation/Cyclization of Indole-3-Carboxamides with KSCN and KSeCN under Mild Conditions
A practical and sustainable photo-induced protocol for the thiocyanation/selenothiocyanation/cyclization of indole-3-carboxamides with cost-effective potassium thiocyanate (KSCN) and potassium selenocyanate (KSeCN) has been developed. This transformation is mediated by the nontoxic organic dye Eosin B and proceeds smoothly at room temperature without the need for metals or bases, offering a practical route to a diverse array of thiocyanated and selenothiocyanated γ-carbolinone derivatives in moderate to good yields (41 examples). Notable advantages include compatibility with gram-scale operations and successful execution under sunlight, which further underscore the synthetic utility of this approach for constructing complex molecular scaffolds.
Authors
- Yucai Tang (ORCID: https://orcid.org/0000-0002-2203-4039)
- Weiguo Zheng
- Dongfang Jiang (ORCID: https://orcid.org/0009-0006-3644-7519)
- Fangyuan Ou
- Na Long
- Weiming Xia
- Kairui Zhang
- Wei-Min He
- Jiale Liu
Institutions
- Changsha Medical University (CN)
- Nanjing Forestry University (CN)
- Hunan University of Arts and Science (CN)
- University of South China (CN)
Publication Details
- Journal
- The Journal of Organic Chemistry
- Published
- 2026-10-19
- DOI
- https://doi.org/10.1021/acs.joc.6c02062
- Primary Topic
- Radical Photochemical Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.00