Synthetic developments on the preparation of sulfides from thiol-free reagents

被引:31
作者
Batista, Gabriel M. F. [1 ,2 ,3 ]
de Castro, Pedro P. [1 ]
dos Santos, Juliana A. [1 ]
Skrydstrup, Troels [2 ,3 ]
Amarante, Giovanni W. [1 ]
机构
[1] Univ Fed Juiz de Fora, Dept Chem, Campus Martelos, BR-36036900 Juiz De Fora, MG, Brazil
[2] Aarhus Univ, Interdisciplinary Nanosci Ctr iNANO, Carbon Dioxide Activat Ctr CADIAC, Gustav Wieds Vej 14, DK-8000 Aarhus C, Denmark
[3] Aarhus Univ, Dept Chem, Gustav Wieds Vej 14, DK-8000 Aarhus C, Denmark
关键词
CATALYZED DIRECT THIOLATION; METAL-FREE SYNTHESIS; C-H BOND; S-S BOND; ELECTRON-RICH ARENES; ARYL METHYL SULFIDES; ELEMENTAL SULFUR; DIARYL DISULFIDES; COUPLING REACTION; OXIDATIVE TRIFLUOROMETHYLTHIOLATION;
D O I
10.1039/d0qo01226b
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Thiols are known for their strong odor and high toxicity, which makes the development of thiol-free alternatives for the construction of sulfur-containing derivatives, in particular sulfides (thioethers), highly desirable. Over the last few years, several approaches for the preparation of these compounds from alternative sources, such as DMSO, disulfides, elemental sulfur, Bunte salts, and N-substituted sulfanylsuccinimides, have been described. This critical review presents an in-depth analysis of the preparation of these derivatives, including the presentation of selected examples and the careful discussion of mechanistic pathways.
引用
收藏
页码:326 / 368
页数:43
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