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- W3136378737 abstract "Herein, we report an efficient protocol for the synthesis of selenated tetracyclic indoloazulenes. The reaction of diorganyl diselenides with molecular iodine in dichloromethane leads to the in situ formation of organo selenenyl iodide. The synthesis of selenylated tetracyclic indoloazulenes through intramolecular cascade cyclization has been achieved via organo selenenyl iodide and bisindole at room temperature under metal-free conditions in good yields. All compounds were fully characterized by the FT-IR, HRMS, and 1H, 13C and 77Se NMR spectral data." @default.
- W3136378737 created "2021-03-29" @default.
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- W3136378737 date "2021-01-01" @default.
- W3136378737 modified "2023-10-17" @default.
- W3136378737 title "Synthesis of selenated tetracyclic indoloazulenes <i>via</i> iodine and diorganyl diselenides" @default.
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- W3136378737 doi "https://doi.org/10.1039/d1ob00268f" @default.
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