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High diastereoselective [4 + 2] annulation of β,γ-unsaturated α-keto esters and p-quinone methides: Approach to polysubstituted 4-aryl chromans and tetrahydroquinolines
Tetrahedron Letters ( IF 1.5 ) Pub Date : 2020-06-30 , DOI: 10.1016/j.tetlet.2020.152171 Wen Si , Fan Xu , Zhanxu Liu , Ran Song , Jian Lv
中文翻译:
β,γ-不饱和α-酮酸酯和对醌甲基化物的非对映选择性[4 + 2]高环化:多取代的4-芳基色氨酸和四氢喹啉的制备方法
更新日期:2020-07-15
Tetrahedron Letters ( IF 1.5 ) Pub Date : 2020-06-30 , DOI: 10.1016/j.tetlet.2020.152171 Wen Si , Fan Xu , Zhanxu Liu , Ran Song , Jian Lv
DBU-mediated [4 + 2] annulation of β,γ-unsaturated α-keto esters and p-quinone methides has been developed. Under mild conditions, the reaction afforded polysubstituted 4-aryl chromans and tetrahydroquinolines as single diastereoisomer in high yields (up to 91% yield) at room temperature.
中文翻译:
β,γ-不饱和α-酮酸酯和对醌甲基化物的非对映选择性[4 + 2]高环化:多取代的4-芳基色氨酸和四氢喹啉的制备方法
已经开发了DBU介导的[4 + 2]的β,γ-不饱和α-酮酯和对醌甲基化物的环化。在温和的条件下,该反应在室温下以高收率(高达91%的收率)提供了多取代的4-芳基苯并二氢吡喃和四氢喹啉,为单一的非对映异构体。