Syntheses of spiro-oxindoles via KI/oxone-mediated oxidation/ cyclization of homotryptamine and homotryptophol derivatives

被引:5
作者
Zheng, Haohao [1 ,2 ]
Chen, Xiangdong [2 ]
Zuo, Jiayu [2 ]
Ye, Jianghai [2 ]
Zhao, Chunsheng [1 ]
Xu, Jun [2 ]
机构
[1] Guizhou Univ, Sch Pharmaceut Sci, Guiyang 550025, Peoples R China
[2] Guizhou Univ Tradit Chinese Med, Sch Pharm, Guiyang 550025, Peoples R China
基金
中国国家自然科学基金;
关键词
Oxidative cyclization; Spiro-oxindoles; Oxone-halide; Hometryptamine; Hometryptophol; STEREOSELECTIVE-SYNTHESIS; AMIDE ALLYLATION; SPIROOXINDOLE; CONSTRUCTION; CATALYSIS; ACID; ANNULATION; DISCOVERY; STRATEGY; UMPOLUNG;
D O I
10.1016/j.tet.2023.133386
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Oxidative cyclization of indoles is one of the most widely used approaches to exploit the synthetic utility of indoles. In continuation of our research interest in green oxidative cyclization of indoles with Oxonehalide. Here we report an oxidative cyclization of hometryptamine and hometryptophol derivatives using KI/oxone, enabling efficiently access to spiro-heterocyclic oxindoles incorporating tetrahydrofurans, pyrrolidines, pyranones, furanones, and lactams would be difficult to prepare by other methods. This protocol features mild reaction condition, green catalytic system, simple operation and broad substrate scope, which can be applied to various potential transformations. (c) 2023 Elsevier Ltd. All rights reserved.
引用
收藏
页数:8
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