钯催化串联Heck环化反应制备氮杂桥环化合物
收稿日期: 2021-04-29
修回日期: 2021-05-11
网络出版日期: 2021-05-25
基金资助
国家自然科学基金(21871240); 中央高校基本科研业务费专项资金(WK2060000017)
Palladium-Catalyzed Tandem Heck Cyclization Reactions to Access the Bridged N-Heterocyclic Compounds
Received date: 2021-04-29
Revised date: 2021-05-11
Online published: 2021-05-25
Supported by
National Natural Science Foundation of China(21871240); Fundamental Research Funds for the Central Universities(WK2060000017)
报道了一种钯催化分子内Heck环化串联反应. 该反应使用3-取代保护的吲哚酰胺衍生物作为原料, 碘化钯作为催化剂, 4-(二甲氨基)三苯基膦作为配体, 在乙腈和甲苯混合溶剂中发生串联反应, 以优良的收率合成了氮杂桥环化合物. 该反应具有良好的官能团兼容性和较高的合成效率, 为“一锅法”构建稠环化合物提供了一种简便的方法.
关键词: 钯催化剂; 分子内Heck串联环化反应; 氮杂桥环化合物; 一锅法
李曼 , 汪颖 , 徐允河 . 钯催化串联Heck环化反应制备氮杂桥环化合物[J]. 有机化学, 2021 , 41(8) : 3073 -3082 . DOI: 10.6023/cjoc202104059
Palladium-catalyzed intramolecular Heck tandem cyclization reactions were developed. With palladium iodide as a catalyst and 4-(dimethylamino)triphenylphosphine as a ligand, 3-substituted indoleamide derivatives were converted to bridged N-heterocyclic products in good yields under simple reaction conditions. The tandem reactions are featured by efficient construction of fused ring compounds in one pot and good functional group compatibility.
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