Back to Search Start Over

The first example of enamine-Lewis acid cooperative bifunctional catalysis: application to the asymmetric aldol reaction.

Authors :
Arnold K
Batsanov AS
Davies B
Grosjean C
Schütz T
Whiting A
Zawatzky K
Source :
Chemical communications (Cambridge, England) [Chem Commun (Camb)] 2008 Sep 07 (33), pp. 3879-81. Date of Electronic Publication: 2008 Jun 24.
Publication Year :
2008

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.

Details

Language :
English
ISSN :
1359-7345
Issue :
33
Database :
MEDLINE
Journal :
Chemical communications (Cambridge, England)
Publication Type :
Academic Journal
Accession number :
18726021
Full Text :
https://doi.org/10.1039/b806779a