Diastereoselective reduction of α-keto esters derived from functionalised cholic acid
| Data(s) |
01/07/1994
|
|---|---|
| Resumo |
The reduction of phenylglyoxalate 2a and pyruvate 2b with LiBH4 in THF at -80 degrees C yield the corresponding alpha-hydroxy esters with ca. 70% diastereoselectivity. |
| Formato |
application/pdf |
| Identificador |
http://eprints.iisc.ernet.in/36405/1/diastereoselective.pdf Maltra, U and Packiarajan, M (1994) Diastereoselective reduction of α-keto esters derived from functionalised cholic acid. In: Tetrahedron: Asymmetry, 5 (7). 1171 -1174 . |
| Publicador |
Elsevier Science |
| Relação |
http://dx.doi.org/10.1016/0957-4166(94)80149-5 http://eprints.iisc.ernet.in/36405/ |
| Palavras-Chave | #Organic Chemistry |
| Tipo |
Editorials/Short Communications PeerReviewed |
