Efficient Catalyst-Free One-Pot Three-Component Synthesis of Novel Spirooxindole Derivatives, and Their Cytotoxic Activities

被引:19
作者
Han, Chao [1 ]
Zhang, Tao [1 ,2 ]
Zhang, Anqi [1 ]
Wang, Dandan [1 ]
Shi, Weimin [1 ]
Tao, Jingchao [1 ]
机构
[1] Zhengzhou Univ, Coll Chem & Mol Engn, Zhengzhou 450052, Henan, Peoples R China
[2] Xinxiang Med Univ, Sch Pharm, Xinxiang 453003, Henan, Peoples R China
来源
SYNTHESIS-STUTTGART | 2014年 / 46卷 / 10期
基金
中国国家自然科学基金;
关键词
polycyclic compounds; heterocyclic compounds; spiro compounds; multicomponent reactions; cytotoxins; MULTICOMPONENT REACTIONS; NATURAL-PRODUCTS; FUNCTIONALIZED SPIROOXINDOLES; STEREOSELECTIVE-SYNTHESIS; ASYMMETRIC-SYNTHESIS; FACILE SYNTHESIS; ACID; CONSTRUCTION; SPIROKETALS; INHIBITORS;
D O I
10.1055/s-0033-1341028
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A simple and efficient one-pot approach for assembling novel spiro[indolepyranopyrrole] derivatives was developed and used to prepare a series of biologically important compounds. The reaction was easily performed with high efficiency under very simple and mild conditions without any catalysts and it gave good yields, avoiding time-consuming costly synthesis and laborious workup and purification of products. The cytotoxic activities of these new spiro[indolepyranopyrrole] derivatives were evaluated in vitro. Most of the tested compounds exhibited significant cytotoxicities to Raji cell lines.
引用
收藏
页码:1389 / 1398
页数:10
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