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Thiourea-catalyzed enantioselective cyanosilylation of ketones.

Journal of the American Chemical Society (2005-06-23)
Douglas E Fuerst, Eric N Jacobsen
ABSTRACT

The new chiral amino thiourea catalyst 3d promotes the highly enantioselective cyanosilylation of a wide variety of ketones. The hindered tertiary amine substituent plays a crucial role with regard to both stereoinduction and reactivity, suggesting a cooperative mechanism involving electrophile activation by thiourea and nucleophile activation by the amine.

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Trimethylsilyl cyanide, 98%
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Sigma-Aldrich
Trimethylsilyl cyanide, technical, ≥95% (GC)
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