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Visible-light induced selenocyclization of 2-ethynylanilines under ambient conditions: simple FeBr3 as a dual-functional catalyst.
Huang, Binbin; Tang, Xinye; Yuan, Jiawei; Zhang, Mingyu; Luo, Zhenyu; Wang, Junlei; Lu, Caicai.
Affiliation
  • Huang B; Faculty of Arts and Sciences/College of Education for the Future, Beijing Normal University, Zhuhai 519085, China. binbinhuang@bnu.edu.cn.
  • Tang X; Faculty of Arts and Sciences/College of Education for the Future, Beijing Normal University, Zhuhai 519085, China. binbinhuang@bnu.edu.cn.
  • Yuan J; Faculty of Arts and Sciences/College of Education for the Future, Beijing Normal University, Zhuhai 519085, China. binbinhuang@bnu.edu.cn.
  • Zhang M; Faculty of Arts and Sciences/College of Education for the Future, Beijing Normal University, Zhuhai 519085, China. binbinhuang@bnu.edu.cn.
  • Luo Z; Faculty of Arts and Sciences/College of Education for the Future, Beijing Normal University, Zhuhai 519085, China. binbinhuang@bnu.edu.cn.
  • Wang J; School of Chemical Engineering, Guizhou Minzu University, Guiyang 550025, China. junleiwang@gzmu.edu.cn.
  • Lu C; Experiment and Practice Innovation Education Center, Beijing Normal University, Zhuhai 519087, China.
Org Biomol Chem ; 22(30): 6198-6204, 2024 Jul 31.
Article in En | MEDLINE | ID: mdl-39028029
ABSTRACT
We report herein a visible-light induced, Fe-catalyzed selenocyclization of 2-ethynylanilines with diselenides under ambient conditions, employing ethyl acetate as a benign solvent with no stoichiometric additive required. The simple iron salt FeBr3 serves as both a photo-induced LMCT (Ligand-to-Metal Charge Transfer) catalyst and a Lewis acid catalyst to promote the desired transformation in a sustainable manner, enabling the facile synthesis of diverse 3-selenylindoles with extended substitution patterns. Moreover, gram-scale reactions and late-stage functionalization of bioactive molecules further highlight the synthetic practicality of this method.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Org Biomol Chem Journal subject: BIOQUIMICA / QUIMICA Year: 2024 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Org Biomol Chem Journal subject: BIOQUIMICA / QUIMICA Year: 2024 Document type: Article Affiliation country: China