Maitra, Uday ; Mathivanan, Packiarajan (1994) Diastereoselective reduction of α-keto esters derived from functionalised cholic acid Tetrahedron: Asymmetry, 5 (7). pp. 1171-1174. ISSN 0957-4166
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Official URL: http://linkinghub.elsevier.com/retrieve/pii/095741...
Related URL: http://dx.doi.org/10.1016/0957-4166(94)80149-5
Abstract
The reduction of phenylglyoxalate 2a and pyruvate 2b with LiBH4 in THF at -80°C yield the corresponding α-hydroxy esters with ca. 70% diastereoselectivity. The reduction of phenylglyoxalate 2a and pyruvate 2b with LiBH4 in THF at -80°C yield the corresponding α-hydroxy esters with ca. 70% diastereoselectivity.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Elsevier Science. |
| ID Code: | 21147 |
| Deposited On: | 20 Nov 2010 09:03 |
| Last Modified: | 20 Nov 2010 09:03 |
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