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  • Cooperative thiourea-Brønsted acid organocatalysis: enantioselective cyanosilylation of aldehydes with TMSCN.

Cooperative thiourea-Brønsted acid organocatalysis: enantioselective cyanosilylation of aldehydes with TMSCN.

The Journal of organic chemistry (2011-10-21)
Zhiguo Zhang, Katharina M Lippert, Heike Hausmann, Mike Kotke, Peter R Schreiner
ABSTRACT

We report a new thiourea-Brønsted acid cooperative catalytic system for the enantioselective cyanosilylation of aldehydes with yields up to 90% and enantioselectivities up to 88%. The addition of an achiral acid was found to be crucial for high asymmetric induction. Mechanistic investigations using a combination of NMR, ESI-MS, and density functional theory computations (including solvent corrections) at the M06/6-31G(d,p) level of theory suggest that the key catalytic species results from the cooperative interaction of bifunctional thioureas and an achiral acid that form well-defined chiral hydrogen-bonding environments.

MATERIALS
Product Number
Brand
Product Description

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