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trimethylsilyl cyanide

Known as: TMSCN 
National Institutes of Health

Papers overview

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2017
2017
A highly efficient copper-catalyzed cyclization/cyanation cascade of unactivated olefins bearing oximes is described. A variety… 
2016
2016
We have developed a one-pot iron-catalysed sequential reaction of secondary amines with primary alcohols, trimethylsilyl cyanide… 
2014
2014
Thiocyanates and trifluoromethyl sulfides are important compounds and have classically been synthesized via multistep procedures… 
Highly Cited
2008
Highly Cited
2008
Novel trans-4-hydroxy-L-proline-derived N,N'-dioxides have been developed and used as efficient organocatalysts for the one-pot… 
2007
2007
Halide or alkoxide free yttrium-salen complexes are excellent catalysts for the ring opening of epoxides mediated by TMSCN and… 
Highly Cited
2006
Highly Cited
2006
N-Heterocyclic carbenes were found to be highly effective organocatalysts in activating TMSCN for facile cyanosilylation of… 
Highly Cited
2000
Highly Cited
2000
Ring-opening reactions of aziridines with trimethylsilyl compounds triggered by tetrabutylammonium fluoride give the… 
Highly Cited
1998
Highly Cited
1998
The past few years have witnessed a profusion of highly efficient, catalytic, enantioand diastereoselective alkylations of…