Iron-Catalyzed Synthesis of Selenoesters from Diselenides and Acyl Chlorides or Acid Anhydrides in the Presence of Magnesium Dust

被引:23
|
作者
Ren, Kai [1 ]
Wang, Min [1 ]
Liu, Ping [1 ]
Wang, Lei [1 ,2 ]
机构
[1] Huaibei Coal Teachers Coll, Dept Chem, Huaibei 235000, Anhui, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organometall Chem, Shanghai 200032, Peoples R China
来源
SYNTHESIS-STUTTGART | 2010年 / 07期
基金
中国国家自然科学基金;
关键词
iron catalyst; magnesium dust; selenoesters; diselenides; acyl chlorides; acid anhydrides; CROSS-COUPLING REACTIONS; GRIGNARD-REAGENTS; REDUCTIVE CLEAVAGE; SELENIUM-COMPOUNDS; SULFIDE OXIDATION; HYDROGEN-PEROXIDE; SE-SE; ESTERS; ARYLATION; DERIVATIVES;
D O I
10.1055/s-0029-1219229
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A novel and efficient synthetic methodology for the iron-catalyzed preparation of selenoesters by the reaction of diselenides with acyl chlorides or acid anhydrides has been developed. In the presence of magnesium dust, iron catalyzes the cleavage of the Se-Se bonds of the diselenides; the subsequent smooth reaction with acyl chlorides or acid anhydrides generates the corresponding selenoesters in good yields. The reaction could be carried out under neutral reaction conditions, and the method is simple, efficient, and practical.
引用
收藏
页码:1078 / 1082
页数:5
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