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Practical, Highly Enantioselective Chemoenzymatic One-Pot Synthesis of Short-Chain Aliphatic β-Amino Acid Esters
| Content Provider | Scilit |
|---|---|
| Author | Gröger, Harald Weiß, Markus |
| Copyright Year | 2009 |
| Description | A practical, highly enantioselective method for the synthesis of short-chain aliphatic β-amino acid esters was developed starting from prochiral and easily accessible substrates. This chemoenzymatic approach is based on a nonenzymatic aza-Michael addition of benzylamine to enoates and subsequent lipase-catalyzed resolution via enantioselective aminolysis. The two reactions are carried out as a one-pot synthesis under solvent free-conditions affording the β-amino esters in satisfying to good yields and with excellent enantioselectivities of up to 99% ee. |
| Related Links | http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0029-1216721.pdf |
| Ending Page | 1254 |
| Page Count | 4 |
| Starting Page | 1251 |
| ISSN | 09365214 |
| e-ISSN | 14372096 |
| DOI | 10.1055/s-0029-1216721 |
| Journal | Synlett |
| Issue Number | 08 |
| Volume Number | 2009 |
| Language | English |
| Publisher | Georg Thieme Verlag KG |
| Publisher Date | 2009-04-08 |
| Access Restriction | Open |
| Subject Keyword | Journal: Synlett Organic Chemistry Amino Acids Asymmetric Catalysis Enzyme Catalysis Stereoselective Synthesis |
| Content Type | Text |
| Resource Type | Article |
| Subject | Organic Chemistry |