Back to Search
Start Over
The first example of enamine-Lewis acid cooperative bifunctional catalysis: application to the asymmetric aldol reaction.
- 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.
- Subjects :
- Catalysis
Acids chemistry
Aldehydes chemistry
Amines chemistry
Lewis Acids chemistry
Subjects
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