Journal
CHEMICAL COMMUNICATIONS
Volume 53, Issue 49, Pages 6577-6580Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c7cc02801f
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Funding
- RWTH Aachen University
- Excellence Initiative of the German federal and state governments
- Fonds der Chemischen Industrie (Sachkostenbeihilfe)
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Slow addition of sodium nitrite allows the in situ preparation of highly explosive diazo compounds and enables their safe and scalable application in iron catalyzed rearrangement reactions of allylic and propargylic sulfides. With catalyst loadings as low as 0.1 mol% an effective entry into alpha-mercapto-nitriles, alpha-mercapto-esters and alpha-trifluoromethyl-sulfides on a gram-scale is achieved.
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