An efficient approach to chloro(organophosphine) gold(I) complexes for the synthesis of auranofin

被引:10
|
作者
Wang, Junchang [1 ]
Mi, Xuemeng [1 ]
Wang, Jiazhe [1 ]
Yang, You [1 ]
机构
[1] East China Univ Sci & Technol, Sch Pharm, Shanghai Key Lab New Drug Design, 130 Meilong Rd, Shanghai 200237, Peoples R China
关键词
GLYCOSYL ORTHO-ALKYNYLBENZOATES; N-HETEROCYCLIC CARBENE; PROPARGYL 1,2-ORTHOESTERS; STEREOSELECTIVE-SYNTHESIS; PHOSPHINE COMPLEXES; ANTITUMOR-ACTIVITY; ANTICANCER; CATALYSIS; DONORS; DRUGS;
D O I
10.1039/c6gc02908f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A practical and efficient synthesis of chloro(organophosphine) gold(I) complexes is reported. Employment of 4,4'-dihydroxydiphenyl sulfide as a safe and non-irritating reductant is highlighted for the generation of Au(I)-S intermediates, which could be trapped by mono-and bidentate phosphine ligands to provide organophosphine gold(I) complexes. The utility of the present method is further demonstrated by the synthesis of the antiarthritic drug auranofin.
引用
收藏
页码:634 / 637
页数:4
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