Transition-Metal-Catalyzed CS Bond Coupling Reaction

Sulfur‐containing molecules such as thioethers are commonly found in chemical biology, organic synthesis, and materials chemistry. While many reliable methods have been developed for preparing these compounds, harsh reaction conditions are usually required in the traditional methods. The transition...

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Published inChemistry, an Asian journal Vol. 9; no. 3; pp. 706 - 722
Main Authors Lee, Chin-Fa, Liu, Yi-Chen, Badsara, Satpal Singh
Format Journal Article
LanguageEnglish
Published Weinheim WILEY-VCH Verlag 01.03.2014
WILEY‐VCH Verlag
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Summary:Sulfur‐containing molecules such as thioethers are commonly found in chemical biology, organic synthesis, and materials chemistry. While many reliable methods have been developed for preparing these compounds, harsh reaction conditions are usually required in the traditional methods. The transition metals have been applied in this field, and the palladium‐catalyzed coupling of thiols with aryl halides and pseudo halides is one of the most important methods in the synthesis of thioethers. Other metals have also been used for the same purpose. Here, we summarize recent efforts in metal‐catalyzed CS bond cross‐coupling reactions, focusing especially on the coupling of thiols with aryl‐ and vinyl halides based on different metals. Feeling cross: In this Focus Review, recent efforts in transition‐metal‐catalyzed CS bond cross‐coupling reactions of thiols with aryl‐ and vinyl halides and pseudo halides are summarized.
Bibliography:National Chung Hsing University
ArticleID:ASIA201301500
National Science Council, Taiwan - No. NSC 101-2113M-005-008-MY3
istex:4F3BB967940D0970C2D8168A1B915C6CF64208AF
ark:/67375/WNG-NWWFM9BR-B
ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-3
content type line 23
ObjectType-Review-1
ISSN:1861-4728
1861-471X
DOI:10.1002/asia.201301500