2022
DOI: 10.1016/j.cclet.2021.08.070
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Iodine-catalyzed amination of benzothiazoles with KSeCN in water to access primary 2-aminobenzothiazoles

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Cited by 14 publications
(2 citation statements)
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“…To our delight, cyclohexanol 2 could be successfully obtained in H 2 O, a solvent widely acknowledged for its abundance, non-toxicity, and environmental compatibility. 59,60 This outcome confirmed our hypothesis that the NHC Rh complex exhibited hydrogenation activity in this vital transformation, even in water. When the reaction was carried out with 0.5 mol% bis-NHC-Rh complex 4, 1 mmol 1, and 5 mol% t-BuONa in H 2 O at 30 °C, 5 bar H 2 for 24 h yielded the highest output of 20%.…”
supporting
confidence: 82%
“…To our delight, cyclohexanol 2 could be successfully obtained in H 2 O, a solvent widely acknowledged for its abundance, non-toxicity, and environmental compatibility. 59,60 This outcome confirmed our hypothesis that the NHC Rh complex exhibited hydrogenation activity in this vital transformation, even in water. When the reaction was carried out with 0.5 mol% bis-NHC-Rh complex 4, 1 mmol 1, and 5 mol% t-BuONa in H 2 O at 30 °C, 5 bar H 2 for 24 h yielded the highest output of 20%.…”
supporting
confidence: 82%
“…Base-metal catalysts have also emerged as potential alternatives to precious metal analogues . In regard to these principles, we have developed chalcogenation and chalcogenocyanation of imidazopyridines as well as amination of benzothiazoles in water . Cu-catalyzed C–H amination and alkylation of imidazopyridines have also been reported .…”
mentioning
confidence: 99%