Prabhu, Kandikere Ramaiah and Devan, Naduthambi and Chandrasekaran, Srinivasan (2002) Chemistry of tetrathiomolybdate: Applications in organic synthesis. In: Synlett (11). pp. 1762-1778.Full text not available from this repository.
The utility of tetrathiomolybdate in a variety of organic transformations is presented in this account. The sulfur transfer ability of tetrathiomolybdate is exploited in the synthesis of organic disulfides under mild reaction conditions. The induced internal redox reactions associated with tetrathiomolybdate have been thoroughly exploited in developing various methodologies, which include the reduction of organic azides, synthesis of diselenides, cyclic imines, thioamides, and thiolactams. In addition, novel deprotection strategies using tetrathiomolybdate have been developed to cleave the propargyl and propargyloxy carbonyl (POC) protecting groups. Tetrathiomolybdate mediated tandem sulfur transfer-reduction-Michael reactions have been applied to the synthesis of sulfur containing bicyclic systems. Furthermore, the reactions in the solid state and the reactions in water medium assisted by tetrathiomolybdate have greatly simplified the synthesis of organic disulfides.
|Item Type:||Journal Article|
|Additional Information:||Copyright of this article belongs to Thieme Medical Publishers.|
|Keywords:||molybdenum;sulfur;tetrathiomolybdate;disulfides;protecting groups;tandem reactions|
|Department/Centre:||Division of Chemical Sciences > Organic Chemistry|
|Date Deposited:||22 Jul 2011 10:02|
|Last Modified:||22 Jul 2011 10:02|
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