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trimethylsilyl cyanide

Known as: TMSCN 
 
National Institutes of Health

Papers overview

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2019
2019
Under mild dual photoredox/copper catalysis, the reaction of N-alkoxypyridinium salts with readily available silyl reagents… Expand
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2013
2013
AbstractReproducible and quantitative gas chromatography–mass spectrometry (GC-MS)-based metabolomics analysis of complex… Expand
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2012
2012
Cyanohydrins are a very important class of compounds in chemistry as well as biology, and have been widely utilized as important… Expand
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2012
2012
The Ni amide and hydroxide complexes [(PCP)Ni(NH(2))] (2; PCP=bis-2,6-di-tert-butylphosphinomethylbenzene) and [(PCP)Ni(OH)] (3… Expand
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2011
2011
The indole alkaloids of the terrestrial blue-green algae[1] have elicited a broad response in the form of new chemical methods… Expand
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2010
2010
A general method for the one-pot, three-component Strecker reaction of ketones was developed using Brønsted acids as… Expand
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2009
2009
Catalyze this! Detailed study of the mechanism of asymmetric cyanohydrin synthesis catalyzed by VO(salen)X complexes (see figure… Expand
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2006
2006
N-Heterocyclic carbenes were found to be highly effective organocatalysts in activating TMSCN for facile cyanosilylation of… Expand
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2006
2006
Cyanohydrin trimethylsilyl ethers are versatile intermediates in the synthesis of α-hydroxy acids and α-amino alcohols. Transfer… Expand
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1998
1998
The past few years have witnessed a profusion of highly efficient, catalytic, enantioand diastereoselective alkylations of… Expand
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