First Highly Diastereoselective Synthesis of s yn α-Methyl β-Fluoroalkyl β-Amino Esters
A new two-step approach for the diastereoselective synthesis of the syn α-methyl β-fluoroalkyl β-amino esters 4 has been developed. This approach is based on the chemical reduction of the fluorinated β-enamino esters 3, which have been previously obtained from imidoyl chlorides 1 and lithium ester e...
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Veröffentlicht in: | Organic letters 1999-10, Vol.1 (7), p.977-980 |
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Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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