Bifunctional chiral urea-containing quaternary ammonium salts can be straightforwardly synthesised in good yield and with high structural diversity a scalable and operationally simple highly telescoped sequence starting from -1,2-cyclohexanediamine. These novel hybrid catalysts were systematically investigated for their potential to control glycine Schiff bases in asymmetric addition reactions. It was found that Michael addition reactions and the herein presented aldol-initiated cascade reaction can be carried out to provide enantiomeric ratios up to 95 : 5 and good yields under mild conditions at room temperature.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4618300PMC
http://dx.doi.org/10.1039/C5RA14466CDOI Listing

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