📜2-(3,5-二甲氧基苯基)苯并呋喃-6-醇置于3-甲基吡啶,三溴化硼,三乙胺体系中,用 5,5-Dimethyl-1,3-Cyclohexadiene,二氯甲烷 作为反应溶剂,化学反应 58.0H,反应生成 桑辛素 D
参考文献:Functional Group Manoeuvring For Tuning Stability And Reactivity: Synthesis Of Cicerfuran,Moracins (D,E,M) And Chromene-Fused Benzofuran-Based Natural Products
标题:Functional Group Manoeuvring For Tuning Stability And Reactivity: Synthesis Of Cicerfuran,Moracins (D,E,M) And Chromene-Fused Benzofuran-Based Natural Products
摘要:作为一种策略,保护基团操纵被应用于调节取代的gem-二溴乙烯酚(12A和22)的稳定性和反应性,用于苯并呋喃类天然产物的多米诺合成(1-8).
DOI:10.1039/c7Ob02459B