The first example of enamine–Lewis acid cooperative bifunctional catalysis: application to the asymmetric Aldol reaction
Kenny Arnold, Andrei S. Batsanov, Bryan W. Davies, Christophe Grosjean, T. Schütz, Andrew Whiting, Kerstin Zawatzky
Abstract
Kenny Arnold, Andrei S. Batsanov, Bryan W. Davies, Christophe Grosjean, T. Schütz, Andrew Whiting, Kerstin Zawatzky
Abstract
(-)-Sparteine directed lithiation of N-Boc-pyrrolidine, alkylation with chloromethylboronate pinacol ester and acid-based deprotection provides homoboroproline HX salt in 94% ee, which is then an efficient enamine-type pyrrolidine catalyst in an asymmetric aldol reaction when neutralised and especially when esterified in situ with a tartrate ester, for example, providing 90% ee of the aldol adduct derived from acetone and p-nitrobenzaldehyde.
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(-)-Sparteine directed lithiation of N-Boc-pyrrolidine, alkylation with chloromethylboronate pinacol ester and acid-based deprotection provides homoboroproline HX salt in 94% ee, which is then an efficient enamine-type pyrrolidine catalyst in an asymmetric aldol reaction when neutralised and especially when esterified in situ with a tartrate ester, for example, providing 90% ee of the aldol adduct derived from acetone and p-nitrobenzaldehyde.
Key concepts: Aldol reaction, Enamine, Chemistry, Pyrrolidine, Adduct, Bifunctional, Lewis acids and bases, Enantioselective synthesis