Iron-Catalyzed Sulfenylation of Indoles with Disulfides Promoted by a Catalytic Amount of Iodine

被引:149
|
作者
Fang, Xiao-Li [1 ]
Tang, Ri-Yuan [1 ]
Zhong, Ping [1 ]
Li, Jin-Heng [1 ]
机构
[1] Wenzhou Univ, Coll Chem & Mat Sci, Wenzhou 325035, Peoples R China
来源
SYNTHESIS-STUTTGART | 2009年 / 24期
基金
中国国家自然科学基金;
关键词
iron(III) fluoride; sulfenylation; indoles; disulfides; sulfenylindoles; iodine; 2ND SULFENYLATION; BIOLOGICAL EVALUATION; DERIVATIVES; 3-SULFENYL; INHIBITORS; MECHANISM;
D O I
10.1055/s-0029-1217037
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Selective sulfenylation of indoles with disulfides using iron(III) fluoride combined with iodine has been developed for the synthesis of sulfenylindoles. In the presence of iron(III) fluoride and iodine, a variety of disulfides underwent the reaction with indoles selectively to afford the corresponding sulfenylindoles in good to excellent yields. Moreover, reactions of indoles with 1,2-diphenyldiselane were also conducted under the same conditions, which smoothly afforded 3-selenylindoles in good yields.
引用
收藏
页码:4183 / 4189
页数:7
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