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Synthesis of Tetraphenyl-furoindoles via Tandem Reactions
Heterocycles ( IF 0.8 ) Pub Date : 2021-06-17 , DOI: 10.3987/com-21-14470 Shi-Yun An , Gao-Xi Jiang , Jin-Long Zhang
Heterocycles ( IF 0.8 ) Pub Date : 2021-06-17 , DOI: 10.3987/com-21-14470 Shi-Yun An , Gao-Xi Jiang , Jin-Long Zhang
We report a novel one-step synthesis of tetraphenyl substituted furoindoles involving acid-catalyzed cascade approach of commercially available m-aminophenols with readily accessible α-hydroxyaldehydes. The tandem reactions involved nucleophilic addition, aldimine condensation, pinacol rearrangement, α-iminol rearrangement, cyclization and dehydration aromatization process. The yield of furoindoles was up to 75%.
中文翻译:
串联反应合成四苯基呋喃吲哚
我们报告涉及市售的酸催化级联途径四苯基取代furoindoles的新型一步法合成米氨基苯酚与易于接近α -hydroxyaldehydes。串联反应涉及亲核加成、醛亚胺缩合、频哪醇重排、α-亚胺醇重排、环化和脱水芳构化过程。呋喃吲哚的产率高达75%。
更新日期:2021-06-17
中文翻译:
串联反应合成四苯基呋喃吲哚
我们报告涉及市售的酸催化级联途径四苯基取代furoindoles的新型一步法合成米氨基苯酚与易于接近α -hydroxyaldehydes。串联反应涉及亲核加成、醛亚胺缩合、频哪醇重排、α-亚胺醇重排、环化和脱水芳构化过程。呋喃吲哚的产率高达75%。