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Chem Commun (Camb) ; (33): 3879-81, 2008 Sep 07.
Article in English | MEDLINE | ID: mdl-18726021

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.


Subject(s)
Acids/chemistry , Aldehydes/chemistry , Amines/chemistry , Lewis Acids/chemistry , Catalysis
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