The first asymmetric silver-catalysed Mukaiyama reaction was reported by Yamagishi and coworkers.1,2 They used a BINOL—AgPF6 complex in aqueous DMF. Yanagisawa and coworkers developed an enantioselective Mukaiyama aldol approach based on the deployment of p-Tol-BINAP—AgF. Trimethoxysilyl enol ethers of ketones were reacted with non-enolizable aldehydes. The corresponding syn-configured aldol adducts were isolated with excellent enantioselectivities (Scheme 3.1.5.1).3,4,5
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(2009). Silver, Palladium and Platinum Lewis Acids. In: Mahrwald, R. (eds) Aldol Reactions. Springer, Dordrecht. https://doi.org/10.1007/978-1-4020-8701-1_12
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